---
-
alleles:
- TTGAATGCCCCAGGTACTCCAAAGCCCTTGCTCTT
- TT
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162561
feature_type: variation
id: rs2068214053
seq_region_name: 22
source: dbSNP
start: 30162527
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162533
feature_type: variation
id: rs1601735665
seq_region_name: 22
source: dbSNP
start: 30162533
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162534
feature_type: variation
id: rs1569343332
seq_region_name: 22
source: dbSNP
start: 30162534
strand: 1
-
alleles:
- CCCC
- CCCCC
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162537
feature_type: variation
id: rs2068214193
seq_region_name: 22
source: dbSNP
start: 30162534
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162539
feature_type: variation
id: rs527981105
seq_region_name: 22
source: dbSNP
start: 30162539
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162543
feature_type: variation
id: rs1259619012
seq_region_name: 22
source: dbSNP
start: 30162543
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162544
feature_type: variation
id: rs73392847
seq_region_name: 22
source: dbSNP
start: 30162544
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162546
feature_type: variation
id: rs1485437870
seq_region_name: 22
source: dbSNP
start: 30162546
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162549
feature_type: variation
id: rs2068214393
seq_region_name: 22
source: dbSNP
start: 30162549
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162551
feature_type: variation
id: rs2147243465
seq_region_name: 22
source: dbSNP
start: 30162551
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162553
feature_type: variation
id: rs1424473044
seq_region_name: 22
source: dbSNP
start: 30162553
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162554
feature_type: variation
id: rs2068214493
seq_region_name: 22
source: dbSNP
start: 30162554
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162555
feature_type: variation
id: rs1207300135
seq_region_name: 22
source: dbSNP
start: 30162555
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162556
feature_type: variation
id: rs1465165702
seq_region_name: 22
source: dbSNP
start: 30162556
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162565
feature_type: variation
id: rs567817219
seq_region_name: 22
source: dbSNP
start: 30162565
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162567
feature_type: variation
id: rs780366559
seq_region_name: 22
source: dbSNP
start: 30162567
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162568
feature_type: variation
id: rs1045208556
seq_region_name: 22
source: dbSNP
start: 30162568
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162569
feature_type: variation
id: rs2068214719
seq_region_name: 22
source: dbSNP
start: 30162569
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162571
feature_type: variation
id: rs748990288
seq_region_name: 22
source: dbSNP
start: 30162571
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162574
feature_type: variation
id: rs138809741
seq_region_name: 22
source: dbSNP
start: 30162574
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162575
feature_type: variation
id: rs1237444658
seq_region_name: 22
source: dbSNP
start: 30162575
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162576
feature_type: variation
id: rs1348092397
seq_region_name: 22
source: dbSNP
start: 30162576
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162577
feature_type: variation
id: rs2068214934
seq_region_name: 22
source: dbSNP
start: 30162577
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162578
feature_type: variation
id: rs1408594595
seq_region_name: 22
source: dbSNP
start: 30162578
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162579
feature_type: variation
id: rs2068215012
seq_region_name: 22
source: dbSNP
start: 30162579
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162585
feature_type: variation
id: rs2147243505
seq_region_name: 22
source: dbSNP
start: 30162585
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162586
feature_type: variation
id: rs1294552893
seq_region_name: 22
source: dbSNP
start: 30162586
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162591
feature_type: variation
id: rs550428027
seq_region_name: 22
source: dbSNP
start: 30162591
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162592
feature_type: variation
id: rs950542931
seq_region_name: 22
source: dbSNP
start: 30162592
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162600
feature_type: variation
id: rs2068215169
seq_region_name: 22
source: dbSNP
start: 30162600
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162602
feature_type: variation
id: rs1882810601
seq_region_name: 22
source: dbSNP
start: 30162602
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162606
feature_type: variation
id: rs1396751907
seq_region_name: 22
source: dbSNP
start: 30162606
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162608
feature_type: variation
id: rs2068215209
seq_region_name: 22
source: dbSNP
start: 30162608
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162609
feature_type: variation
id: rs2068215244
seq_region_name: 22
source: dbSNP
start: 30162609
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162613
feature_type: variation
id: rs1333956742
seq_region_name: 22
source: dbSNP
start: 30162613
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162614
feature_type: variation
id: rs571701609
seq_region_name: 22
source: dbSNP
start: 30162614
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162615
feature_type: variation
id: rs778586260
seq_region_name: 22
source: dbSNP
start: 30162615
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162620
feature_type: variation
id: rs2068215450
seq_region_name: 22
source: dbSNP
start: 30162620
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162621
feature_type: variation
id: rs1188808091
seq_region_name: 22
source: dbSNP
start: 30162621
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162622
feature_type: variation
id: rs1474902369
seq_region_name: 22
source: dbSNP
start: 30162622
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162623
feature_type: variation
id: rs1279350154
seq_region_name: 22
source: dbSNP
start: 30162623
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162625
feature_type: variation
id: rs982839572
seq_region_name: 22
source: dbSNP
start: 30162625
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162626
feature_type: variation
id: rs1015687611
seq_region_name: 22
source: dbSNP
start: 30162626
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162627
feature_type: variation
id: rs2068215634
seq_region_name: 22
source: dbSNP
start: 30162627
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162631
feature_type: variation
id: rs1447952802
seq_region_name: 22
source: dbSNP
start: 30162631
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162633
feature_type: variation
id: rs747615057
seq_region_name: 22
source: dbSNP
start: 30162633
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162635
feature_type: variation
id: rs1261389397
seq_region_name: 22
source: dbSNP
start: 30162635
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162642
feature_type: variation
id: rs1569343383
seq_region_name: 22
source: dbSNP
start: 30162642
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162644
feature_type: variation
id: rs1216237614
seq_region_name: 22
source: dbSNP
start: 30162644
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162645
feature_type: variation
id: rs1355868280
seq_region_name: 22
source: dbSNP
start: 30162645
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162647
feature_type: variation
id: rs1274333486
seq_region_name: 22
source: dbSNP
start: 30162647
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162648
feature_type: variation
id: rs1601735780
seq_region_name: 22
source: dbSNP
start: 30162648
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162650
feature_type: variation
id: rs1601735783
seq_region_name: 22
source: dbSNP
start: 30162650
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162655
feature_type: variation
id: rs2147243582
seq_region_name: 22
source: dbSNP
start: 30162655
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162656
feature_type: variation
id: rs1233413454
seq_region_name: 22
source: dbSNP
start: 30162656
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162657
feature_type: variation
id: rs1333523831
seq_region_name: 22
source: dbSNP
start: 30162657
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162661
feature_type: variation
id: rs1282131612
seq_region_name: 22
source: dbSNP
start: 30162661
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162665
feature_type: variation
id: rs1030171683
seq_region_name: 22
source: dbSNP
start: 30162665
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162666
feature_type: variation
id: rs538799096
seq_region_name: 22
source: dbSNP
start: 30162666
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162672
feature_type: variation
id: rs2068216111
seq_region_name: 22
source: dbSNP
start: 30162672
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162676
feature_type: variation
id: rs17516411
seq_region_name: 22
source: dbSNP
start: 30162676
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162677
feature_type: variation
id: rs1323855604
seq_region_name: 22
source: dbSNP
start: 30162677
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162683
feature_type: variation
id: rs1199481481
seq_region_name: 22
source: dbSNP
start: 30162683
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162685
feature_type: variation
id: rs974474464
seq_region_name: 22
source: dbSNP
start: 30162685
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162691
feature_type: variation
id: rs1601735823
seq_region_name: 22
source: dbSNP
start: 30162691
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162692
feature_type: variation
id: rs1448487060
seq_region_name: 22
source: dbSNP
start: 30162692
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162696
feature_type: variation
id: rs1396648491
seq_region_name: 22
source: dbSNP
start: 30162696
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162697
feature_type: variation
id: rs915955433
seq_region_name: 22
source: dbSNP
start: 30162697
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162699
feature_type: variation
id: rs1601735841
seq_region_name: 22
source: dbSNP
start: 30162699
strand: 1
-
alleles:
- A
- AA
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162699
feature_type: variation
id: rs2068216476
seq_region_name: 22
source: dbSNP
start: 30162699
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162700
feature_type: variation
id: rs2068216508
seq_region_name: 22
source: dbSNP
start: 30162700
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162703
feature_type: variation
id: rs2068216537
seq_region_name: 22
source: dbSNP
start: 30162703
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162705
feature_type: variation
id: rs888938886
seq_region_name: 22
source: dbSNP
start: 30162705
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162710
feature_type: variation
id: rs2068216615
seq_region_name: 22
source: dbSNP
start: 30162710
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162711
feature_type: variation
id: rs970699647
seq_region_name: 22
source: dbSNP
start: 30162711
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162712
feature_type: variation
id: rs2068216709
seq_region_name: 22
source: dbSNP
start: 30162712
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162713
feature_type: variation
id: rs1411646207
seq_region_name: 22
source: dbSNP
start: 30162713
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162715
feature_type: variation
id: rs1193896303
seq_region_name: 22
source: dbSNP
start: 30162715
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162720
feature_type: variation
id: rs981747939
seq_region_name: 22
source: dbSNP
start: 30162720
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162722
feature_type: variation
id: rs2068216784
seq_region_name: 22
source: dbSNP
start: 30162722
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162724
feature_type: variation
id: rs1241917900
seq_region_name: 22
source: dbSNP
start: 30162724
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162726
feature_type: variation
id: rs560353457
seq_region_name: 22
source: dbSNP
start: 30162726
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162727
feature_type: variation
id: rs1191601591
seq_region_name: 22
source: dbSNP
start: 30162727
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162728
feature_type: variation
id: rs2068216948
seq_region_name: 22
source: dbSNP
start: 30162728
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162732
feature_type: variation
id: rs1018756455
seq_region_name: 22
source: dbSNP
start: 30162732
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30162734
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2068217024
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source: dbSNP
start: 30162735
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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source: dbSNP
start: 30162736
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30162737
strand: 1
-
alleles:
- G
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30162740
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
id: rs934848637
seq_region_name: 22
source: dbSNP
start: 30162741
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1215982027
seq_region_name: 22
source: dbSNP
start: 30162742
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30162743
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2068217293
seq_region_name: 22
source: dbSNP
start: 30162744
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30162746
strand: 1
-
alleles:
- GGTGCAGGGGACAAGGCGAA
- GGTGCAGGGGACAAGGCGAATAGGTGCAGGGGACAAGGCGAA
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162765
feature_type: variation
id: rs1269193731
seq_region_name: 22
source: dbSNP
start: 30162746
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs149366985
seq_region_name: 22
source: dbSNP
start: 30162747
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1601735916
seq_region_name: 22
source: dbSNP
start: 30162748
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1402799765
seq_region_name: 22
source: dbSNP
start: 30162751
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2068217535
seq_region_name: 22
source: dbSNP
start: 30162754
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs532577272
seq_region_name: 22
source: dbSNP
start: 30162755
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2068217638
seq_region_name: 22
source: dbSNP
start: 30162757
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162758
feature_type: variation
id: rs947177306
seq_region_name: 22
source: dbSNP
start: 30162758
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162760
feature_type: variation
id: rs2068217719
seq_region_name: 22
source: dbSNP
start: 30162760
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1348240040
seq_region_name: 22
source: dbSNP
start: 30162762
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
id: rs2068217751
seq_region_name: 22
source: dbSNP
start: 30162766
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2068217787
seq_region_name: 22
source: dbSNP
start: 30162770
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2068217825
seq_region_name: 22
source: dbSNP
start: 30162771
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162772
feature_type: variation
id: rs2068217882
seq_region_name: 22
source: dbSNP
start: 30162772
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1039090779
seq_region_name: 22
source: dbSNP
start: 30162774
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162778
feature_type: variation
id: rs1410585030
seq_region_name: 22
source: dbSNP
start: 30162778
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1601735944
seq_region_name: 22
source: dbSNP
start: 30162780
strand: 1
-
alleles:
- TCTCGGGAACCCAGCTGCCCTCGCCCCTCTATCCAC
- "-"
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162815
feature_type: variation
id: rs1419128554
seq_region_name: 22
source: dbSNP
start: 30162780
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2068218031
seq_region_name: 22
source: dbSNP
start: 30162783
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2068218058
seq_region_name: 22
source: dbSNP
start: 30162784
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2068218082
seq_region_name: 22
source: dbSNP
start: 30162785
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs900193800
seq_region_name: 22
source: dbSNP
start: 30162792
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2068218178
seq_region_name: 22
source: dbSNP
start: 30162794
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1601735959
seq_region_name: 22
source: dbSNP
start: 30162795
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2147243762
seq_region_name: 22
source: dbSNP
start: 30162796
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2068218241
seq_region_name: 22
source: dbSNP
start: 30162799
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162801
feature_type: variation
id: rs2068218292
seq_region_name: 22
source: dbSNP
start: 30162801
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs997812452
seq_region_name: 22
source: dbSNP
start: 30162803
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162806
feature_type: variation
id: rs1398652797
seq_region_name: 22
source: dbSNP
start: 30162806
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162808
feature_type: variation
id: rs1284675598
seq_region_name: 22
source: dbSNP
start: 30162808
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162811
feature_type: variation
id: rs1206056370
seq_region_name: 22
source: dbSNP
start: 30162811
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162812
feature_type: variation
id: rs552773490
seq_region_name: 22
source: dbSNP
start: 30162812
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162815
feature_type: variation
id: rs886231933
seq_region_name: 22
source: dbSNP
start: 30162815
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162817
feature_type: variation
id: rs1601735999
seq_region_name: 22
source: dbSNP
start: 30162817
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162818
feature_type: variation
id: rs2068218593
seq_region_name: 22
source: dbSNP
start: 30162818
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162831
feature_type: variation
id: rs572352316
seq_region_name: 22
source: dbSNP
start: 30162831
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162833
feature_type: variation
id: rs1859282677
seq_region_name: 22
source: dbSNP
start: 30162833
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162834
feature_type: variation
id: rs2068218663
seq_region_name: 22
source: dbSNP
start: 30162834
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162841
feature_type: variation
id: rs1004724399
seq_region_name: 22
source: dbSNP
start: 30162841
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162842
feature_type: variation
id: rs1303825034
seq_region_name: 22
source: dbSNP
start: 30162842
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162845
feature_type: variation
id: rs951610185
seq_region_name: 22
source: dbSNP
start: 30162845
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162846
feature_type: variation
id: rs2068218838
seq_region_name: 22
source: dbSNP
start: 30162846
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162848
feature_type: variation
id: rs1233505359
seq_region_name: 22
source: dbSNP
start: 30162848
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162850
feature_type: variation
id: rs2068218907
seq_region_name: 22
source: dbSNP
start: 30162850
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30162852
feature_type: variation
id: rs773081260
seq_region_name: 22
source: dbSNP
start: 30162852
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh37
clinical_significance: []
consequence_type: splice_region_variant
end: 30162853
feature_type: variation
id: rs1281183083
seq_region_name: 22
source: dbSNP
start: 30162853
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 30162858
feature_type: variation
id: rs2068219020
seq_region_name: 22
source: dbSNP
start: 30162858
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: splice_region_variant
end: 30162861
feature_type: variation
id: rs1443111397
seq_region_name: 22
source: dbSNP
start: 30162861
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: splice_region_variant
end: 30162862
feature_type: variation
id: rs918128078
seq_region_name: 22
source: dbSNP
start: 30162862
strand: 1
-
alleles:
- GAG
- "-"
assembly_name: GRCh37
clinical_significance: []
consequence_type: splice_region_variant
end: 30162864
feature_type: variation
id: rs2068219115
seq_region_name: 22
source: dbSNP
start: 30162862
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
end: 30162867
feature_type: variation
id: rs2068219151
seq_region_name: 22
source: dbSNP
start: 30162867
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
end: 30162869
feature_type: variation
id: rs2068219194
seq_region_name: 22
source: dbSNP
start: 30162869
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
end: 30162871
feature_type: variation
id: rs995629805
seq_region_name: 22
source: dbSNP
start: 30162871
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
end: 30162872
feature_type: variation
id: rs948220712
seq_region_name: 22
source: dbSNP
start: 30162872
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
end: 30162873
feature_type: variation
id: rs1436771471
seq_region_name: 22
source: dbSNP
start: 30162873
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
end: 30162874
feature_type: variation
id: rs1023376001
seq_region_name: 22
source: dbSNP
start: 30162874
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
end: 30162877
feature_type: variation
id: rs760681203
seq_region_name: 22
source: dbSNP
start: 30162877
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
end: 30162881
feature_type: variation
id: rs2068219361
seq_region_name: 22
source: dbSNP
start: 30162881
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
end: 30162884
feature_type: variation
id: rs2068219389
seq_region_name: 22
source: dbSNP
start: 30162884
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
end: 30162887
feature_type: variation
id: rs1352646297
seq_region_name: 22
source: dbSNP
start: 30162887
strand: 1
-
alleles:
- T
- A
- C
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
end: 30162888
feature_type: variation
id: rs980572692
seq_region_name: 22
source: dbSNP
start: 30162888
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
end: 30162889
feature_type: variation
id: rs2068219524
seq_region_name: 22
source: dbSNP
start: 30162889
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
end: 30162890
feature_type: variation
id: rs2068219569
seq_region_name: 22
source: dbSNP
start: 30162890
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
end: 30162891
feature_type: variation
id: rs1284964019
seq_region_name: 22
source: dbSNP
start: 30162891
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
end: 30162892
feature_type: variation
id: rs2068219635
seq_region_name: 22
source: dbSNP
start: 30162892
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
end: 30162893
feature_type: variation
id: rs2147243872
seq_region_name: 22
source: dbSNP
start: 30162893
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
end: 30162895
feature_type: variation
id: rs2147243879
seq_region_name: 22
source: dbSNP
start: 30162895
strand: 1
-
alleles:
- AAAA
- AAAAA
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
end: 30162898
feature_type: variation
id: rs2068219674
seq_region_name: 22
source: dbSNP
start: 30162895
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
end: 30162899
feature_type: variation
id: rs536101951
seq_region_name: 22
source: dbSNP
start: 30162899
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
end: 30162900
feature_type: variation
id: rs2068219751
seq_region_name: 22
source: dbSNP
start: 30162900
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
end: 30162901
feature_type: variation
id: rs1179608949
seq_region_name: 22
source: dbSNP
start: 30162901
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
end: 30162902
feature_type: variation
id: rs1486420634
seq_region_name: 22
source: dbSNP
start: 30162902
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
end: 30162903
feature_type: variation
id: rs925021677
seq_region_name: 22
source: dbSNP
start: 30162903
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
end: 30162904
feature_type: variation
id: rs1487284730
seq_region_name: 22
source: dbSNP
start: 30162904
strand: 1
-
alleles:
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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- T
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30162913
strand: 1
-
alleles:
- CCCC
- CCC
assembly_name: GRCh37
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30162913
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
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source: dbSNP
start: 30162915
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30162916
strand: 1
-
alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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source: dbSNP
start: 30162917
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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source: dbSNP
start: 30162918
strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30162919
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh37
clinical_significance: []
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source: dbSNP
start: 30162921
strand: 1
-
alleles:
- G
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assembly_name: GRCh37
clinical_significance: []
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source: dbSNP
start: 30162922
strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh37
clinical_significance: []
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source: dbSNP
start: 30162923
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh37
clinical_significance: []
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source: dbSNP
start: 30162924
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh37
clinical_significance: []
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source: dbSNP
start: 30162926
strand: 1
-
alleles:
- G
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assembly_name: GRCh37
clinical_significance: []
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source: dbSNP
start: 30162929
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh37
clinical_significance: []
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source: dbSNP
start: 30162930
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
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source: dbSNP
start: 30162933
strand: 1
-
alleles:
- G
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assembly_name: GRCh37
clinical_significance: []
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source: dbSNP
start: 30162934
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30162936
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
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source: dbSNP
start: 30162938
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30162939
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30162941
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30162944
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30162945
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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source: dbSNP
start: 30162946
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30162947
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30162948
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30162949
strand: 1
-
alleles:
- T
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
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seq_region_name: 22
source: dbSNP
start: 30162950
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30162951
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30162954
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30162955
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
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source: dbSNP
start: 30162957
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30162958
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30162959
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30162961
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30162963
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh37
clinical_significance: []
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source: dbSNP
start: 30162964
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30162965
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30162966
strand: 1
-
alleles:
- CTCCTCCTCCTGCGTCCTC
- CTCCTCCTCCTGCGTCCTCCTCCTCCTGCGTCCTC
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30162966
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30162967
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
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id: rs1394443565
seq_region_name: 22
source: dbSNP
start: 30162970
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30162973
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30162974
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: non_coding_transcript_exon_variant
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seq_region_name: 22
source: dbSNP
start: 30162980
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30162981
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: non_coding_transcript_exon_variant
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seq_region_name: 22
source: dbSNP
start: 30162983
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30162987
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30162991
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: non_coding_transcript_exon_variant
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source: dbSNP
start: 30162995
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30163001
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30163002
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: regulatory_region_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163003
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: regulatory_region_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163004
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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id: rs2068221694
seq_region_name: 22
source: dbSNP
start: 30163014
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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id: rs1418465732
seq_region_name: 22
source: dbSNP
start: 30163018
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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feature_type: variation
id: rs1305462245
seq_region_name: 22
source: dbSNP
start: 30163019
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: regulatory_region_variant
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id: rs1601736257
seq_region_name: 22
source: dbSNP
start: 30163026
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: regulatory_region_variant
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id: rs933002922
seq_region_name: 22
source: dbSNP
start: 30163031
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
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id: rs1966795134
seq_region_name: 22
source: dbSNP
start: 30163043
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh37
clinical_significance: []
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id: rs1569343561
seq_region_name: 22
source: dbSNP
start: 30163045
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
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end: 30163048
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id: rs1430434571
seq_region_name: 22
source: dbSNP
start: 30163048
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
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id: rs1007791336
seq_region_name: 22
source: dbSNP
start: 30163050
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: regulatory_region_variant
end: 30163053
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id: rs1052079946
seq_region_name: 22
source: dbSNP
start: 30163053
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: regulatory_region_variant
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feature_type: variation
id: rs1016073895
seq_region_name: 22
source: dbSNP
start: 30163054
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: regulatory_region_variant
end: 30163055
feature_type: variation
id: rs2068222004
seq_region_name: 22
source: dbSNP
start: 30163055
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: regulatory_region_variant
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id: rs2068222027
seq_region_name: 22
source: dbSNP
start: 30163056
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: regulatory_region_variant
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id: rs1417863122
seq_region_name: 22
source: dbSNP
start: 30163057
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: regulatory_region_variant
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seq_region_name: 22
source: dbSNP
start: 30163065
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: regulatory_region_variant
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id: rs543189558
seq_region_name: 22
source: dbSNP
start: 30163066
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: regulatory_region_variant
end: 30163067
feature_type: variation
id: rs1421634716
seq_region_name: 22
source: dbSNP
start: 30163067
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: regulatory_region_variant
end: 30163068
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seq_region_name: 22
source: dbSNP
start: 30163068
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: regulatory_region_variant
end: 30163070
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seq_region_name: 22
source: dbSNP
start: 30163070
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: regulatory_region_variant
end: 30163071
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seq_region_name: 22
source: dbSNP
start: 30163071
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: regulatory_region_variant
end: 30163072
feature_type: variation
id: rs1215416634
seq_region_name: 22
source: dbSNP
start: 30163072
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: regulatory_region_variant
end: 30163073
feature_type: variation
id: rs1025656401
seq_region_name: 22
source: dbSNP
start: 30163073
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
end: 30163074
feature_type: variation
id: rs1308286245
seq_region_name: 22
source: dbSNP
start: 30163074
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
end: 30163075
feature_type: variation
id: rs1023068835
seq_region_name: 22
source: dbSNP
start: 30163075
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
end: 30163077
feature_type: variation
id: rs1309526623
seq_region_name: 22
source: dbSNP
start: 30163077
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
end: 30163078
feature_type: variation
id: rs1296532910
seq_region_name: 22
source: dbSNP
start: 30163078
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
end: 30163079
feature_type: variation
id: rs1228204201
seq_region_name: 22
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh37
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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- G
assembly_name: GRCh37
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh37
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feature_type: variation
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seq_region_name: 22
source: dbSNP
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strand: 1
-
alleles:
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- GGGGG
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163085
strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163088
strand: 1
-
alleles:
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- AG
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163089
strand: 1
-
alleles:
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- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163090
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163092
strand: 1
-
alleles:
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- C
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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seq_region_name: 22
source: dbSNP
start: 30163095
strand: 1
-
alleles:
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- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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seq_region_name: 22
source: dbSNP
start: 30163099
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163101
strand: 1
-
alleles:
- G
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assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163104
strand: 1
-
alleles:
- CGA
- CGACGA
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163105
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163110
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163112
strand: 1
-
alleles:
- GGAG
- GGAGGAG
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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feature_type: variation
id: rs1002884328
seq_region_name: 22
source: dbSNP
start: 30163117
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163118
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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feature_type: variation
id: rs2068223010
seq_region_name: 22
source: dbSNP
start: 30163122
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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feature_type: variation
id: rs117507882
seq_region_name: 22
source: dbSNP
start: 30163130
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163133
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163135
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163136
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
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strand: 1
-
alleles:
- T
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163139
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
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strand: 1
-
alleles:
- C
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163145
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163146
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: regulatory_region_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163147
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163148
strand: 1
-
alleles:
- G
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163149
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30163156
strand: 1
-
alleles:
- GG
- G
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163156
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163157
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
id: rs2068223535
seq_region_name: 22
source: dbSNP
start: 30163158
strand: 1
-
alleles:
- AGAAGAA
- AGAA
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163158
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163163
strand: 1
-
alleles:
- AAAAA
- AAAAAA
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163163
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163165
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163166
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163167
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
id: rs1340493847
seq_region_name: 22
source: dbSNP
start: 30163168
strand: 1
-
alleles:
- TT
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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feature_type: variation
id: rs1380123300
seq_region_name: 22
source: dbSNP
start: 30163168
strand: 1
-
alleles:
- T
- A
- G
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163169
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163172
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163174
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30163175
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163180
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163181
strand: 1
-
alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163182
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163184
strand: 1
-
alleles:
- T
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- C
- G
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163185
strand: 1
-
alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
consequence_type: regulatory_region_variant
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feature_type: variation
id: rs2147244235
seq_region_name: 22
source: dbSNP
start: 30163190
strand: 1
-
alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163193
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
id: rs933097453
seq_region_name: 22
source: dbSNP
start: 30163194
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: regulatory_region_variant
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feature_type: variation
id: rs1051714805
seq_region_name: 22
source: dbSNP
start: 30163196
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163197
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: regulatory_region_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163198
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: regulatory_region_variant
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feature_type: variation
id: rs907566020
seq_region_name: 22
source: dbSNP
start: 30163199
strand: 1
-
alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
end: 30163200
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id: rs2068224644
seq_region_name: 22
source: dbSNP
start: 30163200
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
end: 30163203
feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163203
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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seq_region_name: 22
source: dbSNP
start: 30163204
strand: 1
-
alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
end: 30163205
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id: rs2068224729
seq_region_name: 22
source: dbSNP
start: 30163205
strand: 1
-
alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
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feature_type: variation
id: rs1377057932
seq_region_name: 22
source: dbSNP
start: 30163208
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
end: 30163210
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id: rs113818122
seq_region_name: 22
source: dbSNP
start: 30163210
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
end: 30163214
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id: rs1037637750
seq_region_name: 22
source: dbSNP
start: 30163214
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
end: 30163215
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id: rs898971175
seq_region_name: 22
source: dbSNP
start: 30163215
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
end: 30163221
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id: rs1482171937
seq_region_name: 22
source: dbSNP
start: 30163221
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
end: 30163222
feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163222
strand: 1
-
alleles:
- TTTTTTT
- TTTTTT
- TTTTTTTT
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
end: 30163229
feature_type: variation
id: rs140881195
seq_region_name: 22
source: dbSNP
start: 30163223
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
end: 30163228
feature_type: variation
id: rs1212124328
seq_region_name: 22
source: dbSNP
start: 30163228
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
end: 30163229
feature_type: variation
id: rs141881004
seq_region_name: 22
source: dbSNP
start: 30163229
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
end: 30163234
feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163234
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
end: 30163236
feature_type: variation
id: rs2147244305
seq_region_name: 22
source: dbSNP
start: 30163236
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
end: 30163237
feature_type: variation
id: rs2068225052
seq_region_name: 22
source: dbSNP
start: 30163237
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
end: 30163238
feature_type: variation
id: rs1037540361
seq_region_name: 22
source: dbSNP
start: 30163238
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
end: 30163239
feature_type: variation
id: rs1374470884
seq_region_name: 22
source: dbSNP
start: 30163239
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
end: 30163240
feature_type: variation
id: rs532080358
seq_region_name: 22
source: dbSNP
start: 30163240
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
end: 30163245
feature_type: variation
id: rs761860618
seq_region_name: 22
source: dbSNP
start: 30163245
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
end: 30163246
feature_type: variation
id: rs1348294919
seq_region_name: 22
source: dbSNP
start: 30163246
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
end: 30163247
feature_type: variation
id: rs2147244326
seq_region_name: 22
source: dbSNP
start: 30163247
strand: 1
-
alleles:
- A
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
end: 30163248
feature_type: variation
id: rs1314316208
seq_region_name: 22
source: dbSNP
start: 30163248
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: TF_binding_site_variant
end: 30163249
feature_type: variation
id: rs2068225279
seq_region_name: 22
source: dbSNP
start: 30163249
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
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-
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-
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alleles:
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-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh37
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh37
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh37
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alleles:
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assembly_name: GRCh37
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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- T
assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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- G
assembly_name: GRCh37
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strand: 1
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alleles:
- C
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- T
assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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alleles:
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assembly_name: GRCh37
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
- C
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assembly_name: GRCh37
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source: dbSNP
start: 30163342
strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh37
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh37
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start: 30163346
strand: 1
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alleles:
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assembly_name: GRCh37
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source: dbSNP
start: 30163347
strand: 1
-
alleles:
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assembly_name: GRCh37
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alleles:
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assembly_name: GRCh37
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh37
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source: dbSNP
start: 30163351
strand: 1
-
alleles:
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- T
assembly_name: GRCh37
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source: dbSNP
start: 30163352
strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
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source: dbSNP
start: 30163353
strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
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source: dbSNP
start: 30163355
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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source: dbSNP
start: 30163360
strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
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source: dbSNP
start: 30163361
strand: 1
-
alleles:
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- T
assembly_name: GRCh37
clinical_significance: []
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source: dbSNP
start: 30163365
strand: 1
-
alleles:
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- T
assembly_name: GRCh37
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source: dbSNP
start: 30163366
strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
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source: dbSNP
start: 30163367
strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
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source: dbSNP
start: 30163368
strand: 1
-
alleles:
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assembly_name: GRCh37
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source: dbSNP
start: 30163371
strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
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source: dbSNP
start: 30163372
strand: 1
-
alleles:
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- T
assembly_name: GRCh37
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source: dbSNP
start: 30163374
strand: 1
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alleles:
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- G
assembly_name: GRCh37
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source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh37
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source: dbSNP
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strand: 1
-
alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30163377
strand: 1
-
alleles:
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- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
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id: rs987872660
seq_region_name: 22
source: dbSNP
start: 30163378
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
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seq_region_name: 22
source: dbSNP
start: 30163380
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
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id: rs765602001
seq_region_name: 22
source: dbSNP
start: 30163382
strand: 1
-
alleles:
- G
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assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
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feature_type: variation
id: rs2147244535
seq_region_name: 22
source: dbSNP
start: 30163383
strand: 1
-
alleles:
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- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
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seq_region_name: 22
source: dbSNP
start: 30163384
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163385
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
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seq_region_name: 22
source: dbSNP
start: 30163386
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: 5_prime_UTR_variant
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seq_region_name: 22
source: dbSNP
start: 30163387
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: start_lost
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feature_type: variation
id: rs907510198
seq_region_name: 22
source: dbSNP
start: 30163388
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: start_lost
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id: rs2068227623
seq_region_name: 22
source: dbSNP
start: 30163390
strand: 1
-
alleles:
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- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
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seq_region_name: 22
source: dbSNP
start: 30163392
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: synonymous_variant
end: 30163393
feature_type: variation
id: rs369381982
seq_region_name: 22
source: dbSNP
start: 30163393
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163394
feature_type: variation
id: rs1678054911
seq_region_name: 22
source: dbSNP
start: 30163394
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163395
feature_type: variation
id: rs1601736765
seq_region_name: 22
source: dbSNP
start: 30163395
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: synonymous_variant
end: 30163396
feature_type: variation
id: rs767065729
seq_region_name: 22
source: dbSNP
start: 30163396
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163398
feature_type: variation
id: rs1164305036
seq_region_name: 22
source: dbSNP
start: 30163398
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: synonymous_variant
end: 30163399
feature_type: variation
id: rs1416548025
seq_region_name: 22
source: dbSNP
start: 30163399
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163400
feature_type: variation
id: rs750397254
seq_region_name: 22
source: dbSNP
start: 30163400
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163401
feature_type: variation
id: rs756103227
seq_region_name: 22
source: dbSNP
start: 30163401
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: synonymous_variant
end: 30163402
feature_type: variation
id: rs780057933
seq_region_name: 22
source: dbSNP
start: 30163402
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163403
feature_type: variation
id: rs201462074
seq_region_name: 22
source: dbSNP
start: 30163403
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163407
feature_type: variation
id: rs758596969
seq_region_name: 22
source: dbSNP
start: 30163407
strand: 1
-
alleles:
- TCGAAATTGTACTCCCTGCTGT
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: inframe_deletion
end: 30163430
feature_type: variation
id: rs1389875355
seq_region_name: 22
source: dbSNP
start: 30163409
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163410
feature_type: variation
id: rs200929050
seq_region_name: 22
source: dbSNP
start: 30163410
strand: 1
-
alleles:
- A
- C
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: stop_gained
end: 30163412
feature_type: variation
id: rs771003671
seq_region_name: 22
source: dbSNP
start: 30163412
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163413
feature_type: variation
id: rs776636238
seq_region_name: 22
source: dbSNP
start: 30163413
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163414
feature_type: variation
id: rs17849991
seq_region_name: 22
source: dbSNP
start: 30163414
strand: 1
-
alleles:
- ATTGTACTCCCT
- "-"
assembly_name: GRCh37
clinical_significance: []
consequence_type: inframe_deletion
end: 30163425
feature_type: variation
id: rs2068228322
seq_region_name: 22
source: dbSNP
start: 30163414
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: synonymous_variant
end: 30163415
feature_type: variation
id: rs770281965
seq_region_name: 22
source: dbSNP
start: 30163415
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163416
feature_type: variation
id: rs372163897
seq_region_name: 22
source: dbSNP
start: 30163416
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163418
feature_type: variation
id: rs775761012
seq_region_name: 22
source: dbSNP
start: 30163418
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163422
feature_type: variation
id: rs763357633
seq_region_name: 22
source: dbSNP
start: 30163422
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: synonymous_variant
end: 30163423
feature_type: variation
id: rs2068228549
seq_region_name: 22
source: dbSNP
start: 30163423
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: synonymous_variant
end: 30163424
feature_type: variation
id: rs1323991570
seq_region_name: 22
source: dbSNP
start: 30163424
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163425
feature_type: variation
id: rs531285775
seq_region_name: 22
source: dbSNP
start: 30163425
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163427
feature_type: variation
id: rs920467333
seq_region_name: 22
source: dbSNP
start: 30163427
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: synonymous_variant
end: 30163429
feature_type: variation
id: rs377053267
seq_region_name: 22
source: dbSNP
start: 30163429
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163430
feature_type: variation
id: rs1197126192
seq_region_name: 22
source: dbSNP
start: 30163430
strand: 1
-
alleles:
- T
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163431
feature_type: variation
id: rs767192279
seq_region_name: 22
source: dbSNP
start: 30163431
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163432
feature_type: variation
id: rs749945442
seq_region_name: 22
source: dbSNP
start: 30163432
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163433
feature_type: variation
id: rs756156576
seq_region_name: 22
source: dbSNP
start: 30163433
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163434
feature_type: variation
id: rs1416449924
seq_region_name: 22
source: dbSNP
start: 30163434
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: synonymous_variant
end: 30163435
feature_type: variation
id: rs2147244643
seq_region_name: 22
source: dbSNP
start: 30163435
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163436
feature_type: variation
id: rs567943107
seq_region_name: 22
source: dbSNP
start: 30163436
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163437
feature_type: variation
id: rs1457329636
seq_region_name: 22
source: dbSNP
start: 30163437
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163438
feature_type: variation
id: rs1159896297
seq_region_name: 22
source: dbSNP
start: 30163438
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163440
feature_type: variation
id: rs199846630
seq_region_name: 22
source: dbSNP
start: 30163440
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: synonymous_variant
end: 30163441
feature_type: variation
id: rs2068229012
seq_region_name: 22
source: dbSNP
start: 30163441
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163442
feature_type: variation
id: rs1273603511
seq_region_name: 22
source: dbSNP
start: 30163442
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163445
feature_type: variation
id: rs1225864510
seq_region_name: 22
source: dbSNP
start: 30163445
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163446
feature_type: variation
id: rs2068229122
seq_region_name: 22
source: dbSNP
start: 30163446
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163451
feature_type: variation
id: rs536988546
seq_region_name: 22
source: dbSNP
start: 30163451
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 30163452
feature_type: variation
id: rs753668573
seq_region_name: 22
source: dbSNP
start: 30163452
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: synonymous_variant
end: 30163453
feature_type: variation
id: rs754831745
seq_region_name: 22
source: dbSNP
start: 30163453
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: synonymous_variant
end: 30163456
feature_type: variation
id: rs778504097
seq_region_name: 22
source: dbSNP
start: 30163456
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163457
feature_type: variation
id: rs1412798804
seq_region_name: 22
source: dbSNP
start: 30163457
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: synonymous_variant
end: 30163459
feature_type: variation
id: rs1292625891
seq_region_name: 22
source: dbSNP
start: 30163459
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163461
feature_type: variation
id: rs2068229369
seq_region_name: 22
source: dbSNP
start: 30163461
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: synonymous_variant
end: 30163465
feature_type: variation
id: rs369731574
seq_region_name: 22
source: dbSNP
start: 30163465
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163466
feature_type: variation
id: rs1241238334
seq_region_name: 22
source: dbSNP
start: 30163466
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163467
feature_type: variation
id: rs754234891
seq_region_name: 22
source: dbSNP
start: 30163467
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: synonymous_variant
end: 30163468
feature_type: variation
id: rs1259086861
seq_region_name: 22
source: dbSNP
start: 30163468
strand: 1
-
alleles:
- GGG
- GGGG
assembly_name: GRCh37
clinical_significance: []
consequence_type: frameshift_variant
end: 30163470
feature_type: variation
id: rs5844867
seq_region_name: 22
source: dbSNP
start: 30163468
strand: 1
-
alleles:
- CGTCATGTTCTTCGAGCGCGCC
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: inframe_deletion
end: 30163492
feature_type: variation
id: rs757062735
seq_region_name: 22
source: dbSNP
start: 30163471
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163472
feature_type: variation
id: rs757459033
seq_region_name: 22
source: dbSNP
start: 30163472
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163473
feature_type: variation
id: rs781316546
seq_region_name: 22
source: dbSNP
start: 30163473
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163475
feature_type: variation
id: rs2068229731
seq_region_name: 22
source: dbSNP
start: 30163475
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163476
feature_type: variation
id: rs2068229764
seq_region_name: 22
source: dbSNP
start: 30163476
strand: 1
-
alleles:
- T
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163478
feature_type: variation
id: rs887206190
seq_region_name: 22
source: dbSNP
start: 30163478
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163483
feature_type: variation
id: rs745918395
seq_region_name: 22
source: dbSNP
start: 30163483
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163487
feature_type: variation
id: rs770339072
seq_region_name: 22
source: dbSNP
start: 30163487
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163488
feature_type: variation
id: rs1013649125
seq_region_name: 22
source: dbSNP
start: 30163488
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163490
feature_type: variation
id: rs749721393
seq_region_name: 22
source: dbSNP
start: 30163490
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163494
feature_type: variation
id: rs1370365144
seq_region_name: 22
source: dbSNP
start: 30163494
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163495
feature_type: variation
id: rs558714432
seq_region_name: 22
source: dbSNP
start: 30163495
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163496
feature_type: variation
id: rs374152934
seq_region_name: 22
source: dbSNP
start: 30163496
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: stop_gained
end: 30163499
feature_type: variation
id: rs377432442
seq_region_name: 22
source: dbSNP
start: 30163499
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163501
feature_type: variation
id: rs2068230254
seq_region_name: 22
source: dbSNP
start: 30163501
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163503
feature_type: variation
id: rs765767129
seq_region_name: 22
source: dbSNP
start: 30163503
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: synonymous_variant
end: 30163504
feature_type: variation
id: rs2068230316
seq_region_name: 22
source: dbSNP
start: 30163504
strand: 1
-
alleles:
- GCGG
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: inframe_deletion
end: 30163508
feature_type: variation
id: rs780779426
seq_region_name: 22
source: dbSNP
start: 30163505
strand: 1
-
alleles:
- "-"
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: frameshift_variant
end: 30163506
feature_type: variation
id: rs745544773
seq_region_name: 22
source: dbSNP
start: 30163507
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: synonymous_variant
end: 30163507
feature_type: variation
id: rs1191059869
seq_region_name: 22
source: dbSNP
start: 30163507
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163508
feature_type: variation
id: rs1477419274
seq_region_name: 22
source: dbSNP
start: 30163508
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163510
feature_type: variation
id: rs1244427196
seq_region_name: 22
source: dbSNP
start: 30163510
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: synonymous_variant
end: 30163513
feature_type: variation
id: rs753817655
seq_region_name: 22
source: dbSNP
start: 30163513
strand: 1
-
alleles:
- TAT
- TATTAT
assembly_name: GRCh37
clinical_significance: []
consequence_type: inframe_insertion
end: 30163515
feature_type: variation
id: rs755626253
seq_region_name: 22
source: dbSNP
start: 30163513
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163514
feature_type: variation
id: rs576965392
seq_region_name: 22
source: dbSNP
start: 30163514
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163515
feature_type: variation
id: rs1253499683
seq_region_name: 22
source: dbSNP
start: 30163515
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: synonymous_variant
end: 30163516
feature_type: variation
id: rs1351006873
seq_region_name: 22
source: dbSNP
start: 30163516
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163518
feature_type: variation
id: rs1002449165
seq_region_name: 22
source: dbSNP
start: 30163518
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: synonymous_variant
end: 30163519
feature_type: variation
id: rs2068230681
seq_region_name: 22
source: dbSNP
start: 30163519
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163520
feature_type: variation
id: rs2068230707
seq_region_name: 22
source: dbSNP
start: 30163520
strand: 1
-
alleles:
- ACCAC
- AC
assembly_name: GRCh37
clinical_significance: []
consequence_type: inframe_deletion
end: 30163525
feature_type: variation
id: rs779486150
seq_region_name: 22
source: dbSNP
start: 30163521
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: synonymous_variant
end: 30163522
feature_type: variation
id: rs938738477
seq_region_name: 22
source: dbSNP
start: 30163522
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163526
feature_type: variation
id: rs76013375
seq_region_name: 22
source: dbSNP
start: 30163526
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163527
feature_type: variation
id: rs1202833611
seq_region_name: 22
source: dbSNP
start: 30163527
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs2068230926
seq_region_name: 22
source: dbSNP
start: 30163528
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs891757678
seq_region_name: 22
source: dbSNP
start: 30163530
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: synonymous_variant
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feature_type: variation
id: rs1335246004
seq_region_name: 22
source: dbSNP
start: 30163531
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163533
feature_type: variation
id: rs2147244785
seq_region_name: 22
source: dbSNP
start: 30163533
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs552806899
seq_region_name: 22
source: dbSNP
start: 30163534
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163535
feature_type: variation
id: rs2068231063
seq_region_name: 22
source: dbSNP
start: 30163535
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163536
feature_type: variation
id: rs757512157
seq_region_name: 22
source: dbSNP
start: 30163536
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: splice_region_variant
end: 30163537
feature_type: variation
id: rs1043071148
seq_region_name: 22
source: dbSNP
start: 30163537
strand: 1
-
alleles:
- GGTG
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: splice_donor_variant
end: 30163540
feature_type: variation
id: rs1464571918
seq_region_name: 22
source: dbSNP
start: 30163537
strand: 1
-
alleles:
- "-"
- AA
- AAGCT
- AAGCTGTGGAAACACATCAAGCACAA
- AAGCTGTGGAAACACATCAAGCACAAGTAT
- AAGCTGTGGAAACACATCAAGCACAAGTATGAGAACAA
- AAGCTGTGGAAACACATCAAGCACAAGTATGAGAACAAGTA
- AAGCTGTGGAAACACATCAAGCACAAGTATGAGAACAAGTAGTTCCTT
assembly_name: GRCh37
clinical_significance: []
consequence_type: stop_gained
end: 30163537
feature_type: variation
id: rs749795682
seq_region_name: 22
source: dbSNP
start: 30163538
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: splice_donor_variant
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feature_type: variation
id: rs1342988031
seq_region_name: 22
source: dbSNP
start: 30163538
strand: 1
-
alleles:
- "-"
- CTGTGGAAACACATCAAGCACAAGTA
assembly_name: GRCh37
clinical_significance: []
consequence_type: splice_donor_variant
end: 30163538
feature_type: variation
id: rs760862598
seq_region_name: 22
source: dbSNP
start: 30163539
strand: 1
-
alleles:
- G
- GGAAACACATCAAGCACAAGTATGAG
assembly_name: GRCh37
clinical_significance: []
consequence_type: stop_gained
end: 30163540
feature_type: variation
id: rs766473933
seq_region_name: 22
source: dbSNP
start: 30163540
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs372992419
seq_region_name: 22
source: dbSNP
start: 30163542
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163543
feature_type: variation
id: rs750596956
seq_region_name: 22
source: dbSNP
start: 30163543
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163544
feature_type: variation
id: rs779934472
seq_region_name: 22
source: dbSNP
start: 30163544
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163545
feature_type: variation
id: rs1306387107
seq_region_name: 22
source: dbSNP
start: 30163545
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163550
feature_type: variation
id: rs904768837
seq_region_name: 22
source: dbSNP
start: 30163550
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163553
feature_type: variation
id: rs1247734453
seq_region_name: 22
source: dbSNP
start: 30163553
strand: 1
-
alleles:
- A
- AA
assembly_name: GRCh37
clinical_significance: []
consequence_type: frameshift_variant
end: 30163553
feature_type: variation
id: rs1360056841
seq_region_name: 22
source: dbSNP
start: 30163553
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163554
feature_type: variation
id: rs376290630
seq_region_name: 22
source: dbSNP
start: 30163554
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163556
feature_type: variation
id: rs769035451
seq_region_name: 22
source: dbSNP
start: 30163556
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163562
feature_type: variation
id: rs2068231666
seq_region_name: 22
source: dbSNP
start: 30163562
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs1396479309
seq_region_name: 22
source: dbSNP
start: 30163563
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: synonymous_variant
end: 30163570
feature_type: variation
id: rs1452242845
seq_region_name: 22
source: dbSNP
start: 30163570
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: missense_variant
end: 30163571
feature_type: variation
id: rs200176748
seq_region_name: 22
source: dbSNP
start: 30163571
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: stop_lost
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feature_type: variation
id: rs757912322
seq_region_name: 22
source: dbSNP
start: 30163576
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1463397775
seq_region_name: 22
source: dbSNP
start: 30163578
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1296394749
seq_region_name: 22
source: dbSNP
start: 30163579
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 30163581
feature_type: variation
id: rs1395801120
seq_region_name: 22
source: dbSNP
start: 30163581
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 30163582
feature_type: variation
id: rs2147244868
seq_region_name: 22
source: dbSNP
start: 30163582
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 30163584
feature_type: variation
id: rs760337678
seq_region_name: 22
source: dbSNP
start: 30163584
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 30163585
feature_type: variation
id: rs770487443
seq_region_name: 22
source: dbSNP
start: 30163585
strand: 1
-
alleles:
- A
- AA
assembly_name: GRCh37
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 30163585
feature_type: variation
id: rs776505249
seq_region_name: 22
source: dbSNP
start: 30163585
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 30163587
feature_type: variation
id: rs955060788
seq_region_name: 22
source: dbSNP
start: 30163587
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 30163591
feature_type: variation
id: rs775991872
seq_region_name: 22
source: dbSNP
start: 30163591
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: splice_region_variant
end: 30163594
feature_type: variation
id: rs1369018652
seq_region_name: 22
source: dbSNP
start: 30163594
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: splice_region_variant
end: 30163595
feature_type: variation
id: rs1233930121
seq_region_name: 22
source: dbSNP
start: 30163595
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: splice_donor_variant
end: 30163597
feature_type: variation
id: rs374129740
seq_region_name: 22
source: dbSNP
start: 30163597
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 30163600
feature_type: variation
id: rs1339096883
seq_region_name: 22
source: dbSNP
start: 30163600
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: splice_donor_5th_base_variant
end: 30163601
feature_type: variation
id: rs1209372406
seq_region_name: 22
source: dbSNP
start: 30163601
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: splice_region_variant
end: 30163604
feature_type: variation
id: rs777302494
seq_region_name: 22
source: dbSNP
start: 30163604
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163606
feature_type: variation
id: rs2068232206
seq_region_name: 22
source: dbSNP
start: 30163606
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163609
feature_type: variation
id: rs752539369
seq_region_name: 22
source: dbSNP
start: 30163609
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163610
feature_type: variation
id: rs1251278424
seq_region_name: 22
source: dbSNP
start: 30163610
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163613
feature_type: variation
id: rs2068232284
seq_region_name: 22
source: dbSNP
start: 30163613
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163615
feature_type: variation
id: rs1269917402
seq_region_name: 22
source: dbSNP
start: 30163615
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163618
feature_type: variation
id: rs762762515
seq_region_name: 22
source: dbSNP
start: 30163618
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163619
feature_type: variation
id: rs1220786216
seq_region_name: 22
source: dbSNP
start: 30163619
strand: 1
-
alleles:
- "-"
- ATTAAAAGAGAGTTAAAGCCTGATCAATGTCAGAGTCAGAGG
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163622
feature_type: variation
id: rs1213750508
seq_region_name: 22
source: dbSNP
start: 30163623
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163624
feature_type: variation
id: rs763838487
seq_region_name: 22
source: dbSNP
start: 30163624
strand: 1
-
alleles:
- A
- C
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163625
feature_type: variation
id: rs750653186
seq_region_name: 22
source: dbSNP
start: 30163625
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163626
feature_type: variation
id: rs756274550
seq_region_name: 22
source: dbSNP
start: 30163626
strand: 1
-
alleles:
- GGGGG
- GGG
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163634
feature_type: variation
id: rs2147244925
seq_region_name: 22
source: dbSNP
start: 30163630
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163631
feature_type: variation
id: rs370069820
seq_region_name: 22
source: dbSNP
start: 30163631
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163632
feature_type: variation
id: rs779309615
seq_region_name: 22
source: dbSNP
start: 30163632
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163633
feature_type: variation
id: rs1302677237
seq_region_name: 22
source: dbSNP
start: 30163633
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163637
feature_type: variation
id: rs1446250259
seq_region_name: 22
source: dbSNP
start: 30163637
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163638
feature_type: variation
id: rs920500318
seq_region_name: 22
source: dbSNP
start: 30163638
strand: 1
-
alleles:
- GGGG
- GGG
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163641
feature_type: variation
id: rs1168183957
seq_region_name: 22
source: dbSNP
start: 30163638
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163640
feature_type: variation
id: rs532042151
seq_region_name: 22
source: dbSNP
start: 30163640
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163643
feature_type: variation
id: rs1461938334
seq_region_name: 22
source: dbSNP
start: 30163643
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163644
feature_type: variation
id: rs772569226
seq_region_name: 22
source: dbSNP
start: 30163644
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163648
feature_type: variation
id: rs2068232800
seq_region_name: 22
source: dbSNP
start: 30163648
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163650
feature_type: variation
id: rs920295279
seq_region_name: 22
source: dbSNP
start: 30163650
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163654
feature_type: variation
id: rs2068232855
seq_region_name: 22
source: dbSNP
start: 30163654
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163656
feature_type: variation
id: rs1410507063
seq_region_name: 22
source: dbSNP
start: 30163656
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163657
feature_type: variation
id: rs180878075
seq_region_name: 22
source: dbSNP
start: 30163657
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163661
feature_type: variation
id: rs2068232925
seq_region_name: 22
source: dbSNP
start: 30163661
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163662
feature_type: variation
id: rs2068232956
seq_region_name: 22
source: dbSNP
start: 30163662
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163663
feature_type: variation
id: rs2068232980
seq_region_name: 22
source: dbSNP
start: 30163663
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163664
feature_type: variation
id: rs1425143830
seq_region_name: 22
source: dbSNP
start: 30163664
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163665
feature_type: variation
id: rs1414030906
seq_region_name: 22
source: dbSNP
start: 30163665
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163671
feature_type: variation
id: rs776645962
seq_region_name: 22
source: dbSNP
start: 30163671
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163672
feature_type: variation
id: rs1569344104
seq_region_name: 22
source: dbSNP
start: 30163672
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163673
feature_type: variation
id: rs2068233145
seq_region_name: 22
source: dbSNP
start: 30163673
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163675
feature_type: variation
id: rs1482144413
seq_region_name: 22
source: dbSNP
start: 30163675
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163677
feature_type: variation
id: rs2068233192
seq_region_name: 22
source: dbSNP
start: 30163677
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163680
feature_type: variation
id: rs1478723108
seq_region_name: 22
source: dbSNP
start: 30163680
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163681
feature_type: variation
id: rs1191471107
seq_region_name: 22
source: dbSNP
start: 30163681
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163682
feature_type: variation
id: rs1424045909
seq_region_name: 22
source: dbSNP
start: 30163682
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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-
alleles:
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alleles:
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-
alleles:
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-
alleles:
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alleles:
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-
alleles:
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alleles:
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-
alleles:
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assembly_name: GRCh37
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-
alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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start: 30163716
strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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start: 30163739
strand: 1
-
alleles:
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- T
assembly_name: GRCh37
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seq_region_name: 22
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163742
strand: 1
-
alleles:
- "-"
- TGCCACCCTACATACCCA
assembly_name: GRCh37
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consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh37
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh37
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feature_type: variation
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seq_region_name: 22
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strand: 1
-
alleles:
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assembly_name: GRCh37
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feature_type: variation
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seq_region_name: 22
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh37
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feature_type: variation
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seq_region_name: 22
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh37
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
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strand: 1
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alleles:
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- T
assembly_name: GRCh37
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feature_type: variation
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seq_region_name: 22
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30163810
strand: 1
-
alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
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start: 30163811
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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source: dbSNP
start: 30163816
strand: 1
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alleles:
- G
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assembly_name: GRCh37
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seq_region_name: 22
source: dbSNP
start: 30163819
strand: 1
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alleles:
- A
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30163822
strand: 1
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alleles:
- G
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assembly_name: GRCh37
clinical_significance: []
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id: rs894079794
seq_region_name: 22
source: dbSNP
start: 30163825
strand: 1
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alleles:
- C
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30163831
strand: 1
-
alleles:
- A
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- G
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30163833
strand: 1
-
alleles:
- G
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163834
strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
source: dbSNP
start: 30163835
strand: 1
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alleles:
- A
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30163839
strand: 1
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alleles:
- C
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163840
strand: 1
-
alleles:
- C
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163847
strand: 1
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alleles:
- G
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163851
strand: 1
-
alleles:
- G
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163852
strand: 1
-
alleles:
- G
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163853
strand: 1
-
alleles:
- A
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163855
strand: 1
-
alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1051138807
seq_region_name: 22
source: dbSNP
start: 30163858
strand: 1
-
alleles:
- GGG
- GG
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163863
feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163861
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163865
strand: 1
-
alleles:
- A
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2068234879
seq_region_name: 22
source: dbSNP
start: 30163866
strand: 1
-
alleles:
- A
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1601737464
seq_region_name: 22
source: dbSNP
start: 30163868
strand: 1
-
alleles:
- C
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
id: rs1275743554
seq_region_name: 22
source: dbSNP
start: 30163871
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1367175159
seq_region_name: 22
source: dbSNP
start: 30163876
strand: 1
-
alleles:
- CCCC
- CCC
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163879
feature_type: variation
id: rs2068235016
seq_region_name: 22
source: dbSNP
start: 30163876
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2068235047
seq_region_name: 22
source: dbSNP
start: 30163877
strand: 1
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alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163880
feature_type: variation
id: rs1217648075
seq_region_name: 22
source: dbSNP
start: 30163880
strand: 1
-
alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163880
feature_type: variation
id: rs2068235106
seq_region_name: 22
source: dbSNP
start: 30163880
strand: 1
-
alleles:
- C
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163885
feature_type: variation
id: rs1304028855
seq_region_name: 22
source: dbSNP
start: 30163885
strand: 1
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alleles:
- C
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- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163887
feature_type: variation
id: rs1569344157
seq_region_name: 22
source: dbSNP
start: 30163887
strand: 1
-
alleles:
- G
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163891
feature_type: variation
id: rs767543156
seq_region_name: 22
source: dbSNP
start: 30163891
strand: 1
-
alleles:
- C
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163895
feature_type: variation
id: rs2068235235
seq_region_name: 22
source: dbSNP
start: 30163895
strand: 1
-
alleles:
- AA
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163897
feature_type: variation
id: rs1367609146
seq_region_name: 22
source: dbSNP
start: 30163896
strand: 1
-
alleles:
- G
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163900
feature_type: variation
id: rs948165138
seq_region_name: 22
source: dbSNP
start: 30163900
strand: 1
-
alleles:
- C
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163901
feature_type: variation
id: rs1045184304
seq_region_name: 22
source: dbSNP
start: 30163901
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163903
feature_type: variation
id: rs1292593737
seq_region_name: 22
source: dbSNP
start: 30163903
strand: 1
-
alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163906
feature_type: variation
id: rs1569344163
seq_region_name: 22
source: dbSNP
start: 30163906
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163909
feature_type: variation
id: rs2068235365
seq_region_name: 22
source: dbSNP
start: 30163909
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163911
feature_type: variation
id: rs1422322010
seq_region_name: 22
source: dbSNP
start: 30163911
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163915
feature_type: variation
id: rs1371991425
seq_region_name: 22
source: dbSNP
start: 30163915
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163916
feature_type: variation
id: rs2068235430
seq_region_name: 22
source: dbSNP
start: 30163916
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163918
feature_type: variation
id: rs890619017
seq_region_name: 22
source: dbSNP
start: 30163918
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163919
feature_type: variation
id: rs569965271
seq_region_name: 22
source: dbSNP
start: 30163919
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163920
feature_type: variation
id: rs1388321020
seq_region_name: 22
source: dbSNP
start: 30163920
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163922
feature_type: variation
id: rs1676023558
seq_region_name: 22
source: dbSNP
start: 30163922
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163925
feature_type: variation
id: rs532613223
seq_region_name: 22
source: dbSNP
start: 30163925
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163929
feature_type: variation
id: rs2068235535
seq_region_name: 22
source: dbSNP
start: 30163929
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163931
feature_type: variation
id: rs964405204
seq_region_name: 22
source: dbSNP
start: 30163931
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30163933
feature_type: variation
id: rs2068235582
seq_region_name: 22
source: dbSNP
start: 30163933
strand: 1
-
alleles:
- G
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assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh37
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feature_type: variation
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seq_region_name: 22
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strand: 1
-
alleles:
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assembly_name: GRCh37
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seq_region_name: 22
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163956
strand: 1
-
alleles:
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assembly_name: GRCh37
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source: dbSNP
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strand: 1
-
alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
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strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
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strand: 1
-
alleles:
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- G
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
id: rs950615124
seq_region_name: 22
source: dbSNP
start: 30163969
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163970
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs983354927
seq_region_name: 22
source: dbSNP
start: 30163971
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30163973
strand: 1
-
alleles:
- G
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1245587723
seq_region_name: 22
source: dbSNP
start: 30163974
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1487316132
seq_region_name: 22
source: dbSNP
start: 30163981
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2068236066
seq_region_name: 22
source: dbSNP
start: 30163983
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2147245199
seq_region_name: 22
source: dbSNP
start: 30163985
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1601737542
seq_region_name: 22
source: dbSNP
start: 30163987
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1204963640
seq_region_name: 22
source: dbSNP
start: 30163988
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1340469339
seq_region_name: 22
source: dbSNP
start: 30163989
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1842201654
seq_region_name: 22
source: dbSNP
start: 30163990
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs969477733
seq_region_name: 22
source: dbSNP
start: 30163994
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs917105007
seq_region_name: 22
source: dbSNP
start: 30163996
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1234528897
seq_region_name: 22
source: dbSNP
start: 30163999
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2068236268
seq_region_name: 22
source: dbSNP
start: 30164005
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs949896213
seq_region_name: 22
source: dbSNP
start: 30164007
strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1300044989
seq_region_name: 22
source: dbSNP
start: 30164011
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164014
feature_type: variation
id: rs2068236360
seq_region_name: 22
source: dbSNP
start: 30164014
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
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end: 30164016
feature_type: variation
id: rs2068236378
seq_region_name: 22
source: dbSNP
start: 30164016
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1180102841
seq_region_name: 22
source: dbSNP
start: 30164019
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1352015010
seq_region_name: 22
source: dbSNP
start: 30164024
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2068236452
seq_region_name: 22
source: dbSNP
start: 30164030
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2068236476
seq_region_name: 22
source: dbSNP
start: 30164032
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1601737566
seq_region_name: 22
source: dbSNP
start: 30164033
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164035
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs982633416
seq_region_name: 22
source: dbSNP
start: 30164040
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164042
feature_type: variation
id: rs2068236580
seq_region_name: 22
source: dbSNP
start: 30164042
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164043
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1601737575
seq_region_name: 22
source: dbSNP
start: 30164048
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164049
feature_type: variation
id: rs2068236669
seq_region_name: 22
source: dbSNP
start: 30164049
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164050
feature_type: variation
id: rs2068236699
seq_region_name: 22
source: dbSNP
start: 30164050
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164051
feature_type: variation
id: rs1380722565
seq_region_name: 22
source: dbSNP
start: 30164051
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164054
feature_type: variation
id: rs2068236748
seq_region_name: 22
source: dbSNP
start: 30164054
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1393995131
seq_region_name: 22
source: dbSNP
start: 30164057
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164059
feature_type: variation
id: rs1438843807
seq_region_name: 22
source: dbSNP
start: 30164059
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164064
feature_type: variation
id: rs535363240
seq_region_name: 22
source: dbSNP
start: 30164064
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164070
feature_type: variation
id: rs926739852
seq_region_name: 22
source: dbSNP
start: 30164070
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164087
feature_type: variation
id: rs938073158
seq_region_name: 22
source: dbSNP
start: 30164087
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164089
feature_type: variation
id: rs2068236921
seq_region_name: 22
source: dbSNP
start: 30164089
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164090
feature_type: variation
id: rs2068236946
seq_region_name: 22
source: dbSNP
start: 30164090
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164094
feature_type: variation
id: rs1053714294
seq_region_name: 22
source: dbSNP
start: 30164094
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164100
feature_type: variation
id: rs1405816205
seq_region_name: 22
source: dbSNP
start: 30164100
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164101
feature_type: variation
id: rs1569344214
seq_region_name: 22
source: dbSNP
start: 30164101
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164107
feature_type: variation
id: rs893772817
seq_region_name: 22
source: dbSNP
start: 30164107
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164113
feature_type: variation
id: rs1376966194
seq_region_name: 22
source: dbSNP
start: 30164113
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164114
feature_type: variation
id: rs2068237109
seq_region_name: 22
source: dbSNP
start: 30164114
strand: 1
-
alleles:
- CC
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164120
feature_type: variation
id: rs960644109
seq_region_name: 22
source: dbSNP
start: 30164119
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164130
feature_type: variation
id: rs987929639
seq_region_name: 22
source: dbSNP
start: 30164130
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164140
feature_type: variation
id: rs2068237211
seq_region_name: 22
source: dbSNP
start: 30164140
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164141
feature_type: variation
id: rs766874938
seq_region_name: 22
source: dbSNP
start: 30164141
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164147
feature_type: variation
id: rs1601737625
seq_region_name: 22
source: dbSNP
start: 30164147
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164148
feature_type: variation
id: rs2147245293
seq_region_name: 22
source: dbSNP
start: 30164148
strand: 1
-
alleles:
- AA
- AAA
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164153
feature_type: variation
id: rs913759149
seq_region_name: 22
source: dbSNP
start: 30164152
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164154
feature_type: variation
id: rs945664103
seq_region_name: 22
source: dbSNP
start: 30164154
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164162
feature_type: variation
id: rs1043549382
seq_region_name: 22
source: dbSNP
start: 30164162
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164163
feature_type: variation
id: rs1601737632
seq_region_name: 22
source: dbSNP
start: 30164163
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164165
feature_type: variation
id: rs2068237414
seq_region_name: 22
source: dbSNP
start: 30164165
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164171
feature_type: variation
id: rs2068237434
seq_region_name: 22
source: dbSNP
start: 30164171
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164172
feature_type: variation
id: rs1201360034
seq_region_name: 22
source: dbSNP
start: 30164172
strand: 1
-
alleles:
- T
- TCGT
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164179
feature_type: variation
id: rs2068237490
seq_region_name: 22
source: dbSNP
start: 30164179
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164180
feature_type: variation
id: rs2068237527
seq_region_name: 22
source: dbSNP
start: 30164180
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164183
feature_type: variation
id: rs1483238826
seq_region_name: 22
source: dbSNP
start: 30164183
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164184
feature_type: variation
id: rs1254758023
seq_region_name: 22
source: dbSNP
start: 30164184
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164185
feature_type: variation
id: rs2068237599
seq_region_name: 22
source: dbSNP
start: 30164185
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164186
feature_type: variation
id: rs2068237630
seq_region_name: 22
source: dbSNP
start: 30164186
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164193
feature_type: variation
id: rs925954406
seq_region_name: 22
source: dbSNP
start: 30164193
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164194
feature_type: variation
id: rs1333614264
seq_region_name: 22
source: dbSNP
start: 30164194
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164195
feature_type: variation
id: rs1288603948
seq_region_name: 22
source: dbSNP
start: 30164195
strand: 1
-
alleles:
- CCACATGCCTGGTAGGTGGTACCAC
- CCACATGCCTGGTAGGTGGTACCACATGCCTGGTAGGTGGTACCAC
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164221
feature_type: variation
id: rs1378191454
seq_region_name: 22
source: dbSNP
start: 30164197
strand: 1
-
alleles:
- CACA
- CACACA
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164201
feature_type: variation
id: rs1446526922
seq_region_name: 22
source: dbSNP
start: 30164198
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164202
feature_type: variation
id: rs1333796695
seq_region_name: 22
source: dbSNP
start: 30164202
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164203
feature_type: variation
id: rs931980203
seq_region_name: 22
source: dbSNP
start: 30164203
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164204
feature_type: variation
id: rs2068237844
seq_region_name: 22
source: dbSNP
start: 30164204
strand: 1
-
alleles:
- GGTAGGT
- GGT
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164213
feature_type: variation
id: rs1396369761
seq_region_name: 22
source: dbSNP
start: 30164207
strand: 1
-
alleles:
- T
- C
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strand: 1
-
alleles:
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-
alleles:
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strand: 1
-
alleles:
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh37
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source: dbSNP
start: 30164264
strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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strand: 1
-
alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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strand: 1
-
alleles:
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assembly_name: GRCh37
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source: dbSNP
start: 30164327
strand: 1
-
alleles:
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- G
assembly_name: GRCh37
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strand: 1
-
alleles:
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assembly_name: GRCh37
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
source: dbSNP
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strand: 1
-
alleles:
- C
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assembly_name: GRCh37
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seq_region_name: 22
source: dbSNP
start: 30164341
strand: 1
-
alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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start: 30164342
strand: 1
-
alleles:
- T
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assembly_name: GRCh37
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
source: dbSNP
start: 30164359
strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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strand: 1
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alleles:
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- T
assembly_name: GRCh37
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seq_region_name: 22
source: dbSNP
start: 30164369
strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30164373
strand: 1
-
alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30164374
strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
source: dbSNP
start: 30164376
strand: 1
-
alleles:
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assembly_name: GRCh37
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seq_region_name: 22
source: dbSNP
start: 30164378
strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30164379
strand: 1
-
alleles:
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- G
assembly_name: GRCh37
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seq_region_name: 22
source: dbSNP
start: 30164380
strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
source: dbSNP
start: 30164381
strand: 1
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alleles:
- C
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164384
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30164387
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30164390
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30164391
strand: 1
-
alleles:
- A
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30164399
strand: 1
-
alleles:
- ACTT
- "-"
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30164399
strand: 1
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alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30164401
strand: 1
-
alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30164402
strand: 1
-
alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30164407
strand: 1
-
alleles:
- TTTAATTT
- TTT
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164408
strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 22
source: dbSNP
start: 30164416
strand: 1
-
alleles:
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- CTG
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164420
strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164421
strand: 1
-
alleles:
- G
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164422
strand: 1
-
alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164423
strand: 1
-
alleles:
- G
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164426
strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164427
strand: 1
-
alleles:
- CTCT
- CT
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164428
strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164432
strand: 1
-
alleles:
- G
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164435
feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164435
strand: 1
-
alleles:
- C
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
id: rs1342615878
seq_region_name: 22
source: dbSNP
start: 30164436
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164438
strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164439
strand: 1
-
alleles:
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- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164442
feature_type: variation
id: rs2068240159
seq_region_name: 22
source: dbSNP
start: 30164442
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164443
feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164443
strand: 1
-
alleles:
- G
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164444
feature_type: variation
id: rs2068240193
seq_region_name: 22
source: dbSNP
start: 30164444
strand: 1
-
alleles:
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- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164448
feature_type: variation
id: rs967876310
seq_region_name: 22
source: dbSNP
start: 30164448
strand: 1
-
alleles:
- AGTG
- AGTGAGTG
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164460
feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164457
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164459
feature_type: variation
id: rs1230313700
seq_region_name: 22
source: dbSNP
start: 30164459
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30164463
feature_type: variation
id: rs2068240320
seq_region_name: 22
source: dbSNP
start: 30164463
strand: 1
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alleles:
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alleles:
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alleles:
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-
alleles:
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alleles:
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alleles:
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alleles:
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strand: 1
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alleles:
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alleles:
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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seq_region_name: 22
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh37
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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alleles:
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assembly_name: GRCh37
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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start: 30164601
strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164607
strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
source: dbSNP
start: 30164611
strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
source: dbSNP
start: 30164612
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164612
strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
source: dbSNP
start: 30164613
strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
source: dbSNP
start: 30164613
strand: 1
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alleles:
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assembly_name: GRCh37
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164613
strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30164614
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30164615
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30164615
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164615
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30164616
strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
source: dbSNP
start: 30164616
strand: 1
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alleles:
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assembly_name: GRCh37
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164616
strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
source: dbSNP
start: 30164616
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164617
strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
source: dbSNP
start: 30164617
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164618
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164618
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164619
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164619
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164620
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30164620
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164621
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30164621
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30164622
strand: 1
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alleles:
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- TTT
- TTTTT
- TTTTTT
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164622
strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164623
strand: 1
-
alleles:
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assembly_name: GRCh37
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh37
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alleles:
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strand: 1
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alleles:
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strand: 1
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alleles:
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alleles:
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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strand: 1
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alleles:
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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alleles:
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assembly_name: GRCh37
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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start: 30164815
strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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start: 30164816
strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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start: 30164820
strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
source: dbSNP
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strand: 1
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assembly_name: GRCh37
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seq_region_name: 22
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start: 30164828
strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
source: dbSNP
start: 30164829
strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
source: dbSNP
start: 30164843
strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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start: 30164844
strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
source: dbSNP
start: 30164849
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30164857
strand: 1
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alleles:
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assembly_name: GRCh37
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164865
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30164872
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30164873
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164874
strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30164882
strand: 1
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- C
assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164886
strand: 1
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- T
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30164891
strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164895
strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30164896
strand: 1
-
alleles:
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- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30164896
strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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strand: 1
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alleles:
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strand: 1
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alleles:
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-
alleles:
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strand: 1
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alleles:
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assembly_name: GRCh37
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alleles:
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assembly_name: GRCh37
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alleles:
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh37
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
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feature_type: variation
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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start: 30165028
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alleles:
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assembly_name: GRCh37
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start: 30165031
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alleles:
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assembly_name: GRCh37
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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start: 30165037
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30165040
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
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start: 30165050
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
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start: 30165055
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30165060
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
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start: 30165061
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30165068
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30165072
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30165078
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 22
source: dbSNP
start: 30165081
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30165085
strand: 1
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alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30165086
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1211699949
seq_region_name: 22
source: dbSNP
start: 30165090
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30165091
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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id: rs2068246425
seq_region_name: 22
source: dbSNP
start: 30165096
strand: 1
-
alleles:
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- CC
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165098
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seq_region_name: 22
source: dbSNP
start: 30165096
strand: 1
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alleles:
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- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 22
source: dbSNP
start: 30165098
strand: 1
-
alleles:
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- CTCAA
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165108
feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30165098
strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30165106
strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30165111
strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30165116
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165120
feature_type: variation
id: rs1019046701
seq_region_name: 22
source: dbSNP
start: 30165120
strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165123
feature_type: variation
id: rs1351918178
seq_region_name: 22
source: dbSNP
start: 30165123
strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2068246592
seq_region_name: 22
source: dbSNP
start: 30165126
strand: 1
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alleles:
- T
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- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165127
feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30165127
strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165130
feature_type: variation
id: rs1232016419
seq_region_name: 22
source: dbSNP
start: 30165130
strand: 1
-
alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs868129313
seq_region_name: 22
source: dbSNP
start: 30165133
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165136
feature_type: variation
id: rs1732671989
seq_region_name: 22
source: dbSNP
start: 30165136
strand: 1
-
alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30165141
strand: 1
-
alleles:
- ACTTACTT
- ACTT
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165152
feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30165145
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2068246721
seq_region_name: 22
source: dbSNP
start: 30165149
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165155
feature_type: variation
id: rs1304452126
seq_region_name: 22
source: dbSNP
start: 30165155
strand: 1
-
alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165163
feature_type: variation
id: rs2147246149
seq_region_name: 22
source: dbSNP
start: 30165163
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165165
feature_type: variation
id: rs2068246739
seq_region_name: 22
source: dbSNP
start: 30165165
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165166
feature_type: variation
id: rs2068246755
seq_region_name: 22
source: dbSNP
start: 30165166
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165171
feature_type: variation
id: rs2068246773
seq_region_name: 22
source: dbSNP
start: 30165171
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165173
feature_type: variation
id: rs2068246799
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strand: 1
-
alleles:
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-
alleles:
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-
alleles:
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strand: 1
-
alleles:
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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alleles:
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strand: 1
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alleles:
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strand: 1
-
alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
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strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30165234
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
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strand: 1
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alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh37
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feature_type: variation
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seq_region_name: 22
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strand: 1
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alleles:
- T
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assembly_name: GRCh37
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh37
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feature_type: variation
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seq_region_name: 22
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strand: 1
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alleles:
- GG
- G
assembly_name: GRCh37
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feature_type: variation
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strand: 1
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alleles:
- T
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assembly_name: GRCh37
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seq_region_name: 22
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strand: 1
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alleles:
- G
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assembly_name: GRCh37
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source: dbSNP
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strand: 1
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alleles:
- C
- T
assembly_name: GRCh37
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feature_type: variation
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seq_region_name: 22
source: dbSNP
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strand: 1
-
alleles:
- G
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30165312
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30165322
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30165325
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
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start: 30165327
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
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start: 30165330
strand: 1
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alleles:
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assembly_name: GRCh37
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strand: 1
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alleles:
- C
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assembly_name: GRCh37
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30165348
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30165353
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30165354
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30165355
strand: 1
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alleles:
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- G
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30165357
strand: 1
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alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
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id: rs2147246222
seq_region_name: 22
source: dbSNP
start: 30165358
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30165360
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30165361
strand: 1
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alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30165362
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30165363
strand: 1
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alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
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id: rs1327037614
seq_region_name: 22
source: dbSNP
start: 30165370
strand: 1
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alleles:
- G
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30165372
strand: 1
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alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30165379
strand: 1
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alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30165380
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
id: rs2068247974
seq_region_name: 22
source: dbSNP
start: 30165384
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30165397
strand: 1
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alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30165401
strand: 1
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alleles:
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- T
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30165404
strand: 1
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alleles:
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- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 22
source: dbSNP
start: 30165405
strand: 1
-
alleles:
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assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30165410
strand: 1
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alleles:
- A
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- G
assembly_name: GRCh37
clinical_significance: []
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seq_region_name: 22
source: dbSNP
start: 30165412
strand: 1
-
alleles:
- G
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30165416
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30165417
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30165421
strand: 1
-
alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 22
source: dbSNP
start: 30165423
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2068248208
seq_region_name: 22
source: dbSNP
start: 30165427
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165434
feature_type: variation
id: rs541753666
seq_region_name: 22
source: dbSNP
start: 30165434
strand: 1
-
alleles:
- G
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1019497594
seq_region_name: 22
source: dbSNP
start: 30165435
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165438
feature_type: variation
id: rs2077035112
seq_region_name: 22
source: dbSNP
start: 30165438
strand: 1
-
alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165439
feature_type: variation
id: rs1444967596
seq_region_name: 22
source: dbSNP
start: 30165439
strand: 1
-
alleles:
- T
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165448
feature_type: variation
id: rs2147246254
seq_region_name: 22
source: dbSNP
start: 30165448
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165451
feature_type: variation
id: rs1018980598
seq_region_name: 22
source: dbSNP
start: 30165451
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165454
feature_type: variation
id: rs2068248313
seq_region_name: 22
source: dbSNP
start: 30165454
strand: 1
-
alleles:
- G
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165457
feature_type: variation
id: rs562925841
seq_region_name: 22
source: dbSNP
start: 30165457
strand: 1
-
alleles:
- G
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assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165463
feature_type: variation
id: rs2068248363
seq_region_name: 22
source: dbSNP
start: 30165463
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165464
feature_type: variation
id: rs1223034591
seq_region_name: 22
source: dbSNP
start: 30165464
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165465
feature_type: variation
id: rs1490106013
seq_region_name: 22
source: dbSNP
start: 30165465
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165467
feature_type: variation
id: rs975016878
seq_region_name: 22
source: dbSNP
start: 30165467
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165469
feature_type: variation
id: rs777508981
seq_region_name: 22
source: dbSNP
start: 30165469
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165470
feature_type: variation
id: rs2068248464
seq_region_name: 22
source: dbSNP
start: 30165470
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165472
feature_type: variation
id: rs2068248484
seq_region_name: 22
source: dbSNP
start: 30165472
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165473
feature_type: variation
id: rs765568672
seq_region_name: 22
source: dbSNP
start: 30165473
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165480
feature_type: variation
id: rs993607915
seq_region_name: 22
source: dbSNP
start: 30165480
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165481
feature_type: variation
id: rs749055546
seq_region_name: 22
source: dbSNP
start: 30165481
strand: 1
-
alleles:
- AAAAAAAAAA
- AAAAAAAAA
- AAAAAAAAAAA
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165495
feature_type: variation
id: rs952095644
seq_region_name: 22
source: dbSNP
start: 30165486
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165491
feature_type: variation
id: rs2068248620
seq_region_name: 22
source: dbSNP
start: 30165491
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165497
feature_type: variation
id: rs2147246282
seq_region_name: 22
source: dbSNP
start: 30165497
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165499
feature_type: variation
id: rs2147246283
seq_region_name: 22
source: dbSNP
start: 30165499
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165500
feature_type: variation
id: rs2147246285
seq_region_name: 22
source: dbSNP
start: 30165500
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165506
feature_type: variation
id: rs1179693345
seq_region_name: 22
source: dbSNP
start: 30165506
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165520
feature_type: variation
id: rs1303921542
seq_region_name: 22
source: dbSNP
start: 30165520
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh37
clinical_significance: []
consequence_type: intron_variant
end: 30165521
feature_type: variation
id: rs1237904055
seq_region_name: 22
source: dbSNP
start: 30165521
strand: 1