--- - 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 end: 30162734 feature_type: variation id: rs2047355929 seq_region_name: 22 source: dbSNP start: 30162734 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30162735 feature_type: variation id: rs2068217024 seq_region_name: 22 source: dbSNP start: 30162735 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30162736 feature_type: variation id: rs1466764070 seq_region_name: 22 source: dbSNP start: 30162736 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30162737 feature_type: variation id: rs2068217105 seq_region_name: 22 source: dbSNP start: 30162737 strand: 1 - alleles: - G - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30162740 feature_type: variation id: rs1172191667 seq_region_name: 22 source: dbSNP start: 30162740 strand: 1 - alleles: - G - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30162741 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 end: 30162742 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 end: 30162743 feature_type: variation id: rs2068217258 seq_region_name: 22 source: dbSNP start: 30162743 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30162744 feature_type: variation id: rs2068217293 seq_region_name: 22 source: dbSNP start: 30162744 strand: 1 - alleles: - G - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30162746 feature_type: variation id: rs1225984518 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 end: 30162747 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 end: 30162748 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 end: 30162751 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 end: 30162754 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 end: 30162755 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 end: 30162757 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 end: 30162762 feature_type: variation id: rs1348240040 seq_region_name: 22 source: dbSNP start: 30162762 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30162766 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 end: 30162770 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 end: 30162771 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 end: 30162774 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 end: 30162780 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 end: 30162783 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 end: 30162784 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 end: 30162785 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 end: 30162792 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 end: 30162794 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 end: 30162795 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 end: 30162796 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 end: 30162799 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 end: 30162803 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: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162909 feature_type: variation id: rs1310216316 seq_region_name: 22 source: dbSNP start: 30162909 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162912 feature_type: variation id: rs2068219983 seq_region_name: 22 source: dbSNP start: 30162912 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162913 feature_type: variation id: rs770886387 seq_region_name: 22 source: dbSNP start: 30162913 strand: 1 - alleles: - CCCC - CCC assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162916 feature_type: variation id: rs1224565392 seq_region_name: 22 source: dbSNP start: 30162913 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162915 feature_type: variation id: rs2068220079 seq_region_name: 22 source: dbSNP start: 30162915 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162916 feature_type: variation id: rs1286332402 seq_region_name: 22 source: dbSNP start: 30162916 strand: 1 - alleles: - T - A assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162917 feature_type: variation id: rs1224218090 seq_region_name: 22 source: dbSNP start: 30162917 strand: 1 - alleles: - C - A assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162918 feature_type: variation id: rs776541905 seq_region_name: 22 source: dbSNP start: 30162918 strand: 1 - alleles: - G - C assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162919 feature_type: variation id: rs1372711458 seq_region_name: 22 source: dbSNP start: 30162919 strand: 1 - alleles: - C - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162921 feature_type: variation id: rs1286475125 seq_region_name: 22 source: dbSNP start: 30162921 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162922 feature_type: variation id: rs982078851 seq_region_name: 22 source: dbSNP start: 30162922 strand: 1 - alleles: - T - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162923 feature_type: variation id: rs2068220335 seq_region_name: 22 source: dbSNP start: 30162923 strand: 1 - alleles: - C - A assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162924 feature_type: variation id: rs2068220373 seq_region_name: 22 source: dbSNP start: 30162924 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162926 feature_type: variation id: rs1356379479 seq_region_name: 22 source: dbSNP start: 30162926 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162929 feature_type: variation id: rs928893859 seq_region_name: 22 source: dbSNP start: 30162929 strand: 1 - alleles: - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: splice_region_variant end: 30162930 feature_type: variation id: rs1433812656 seq_region_name: 22 source: dbSNP start: 30162930 strand: 1 - alleles: - G - C assembly_name: GRCh37 clinical_significance: [] consequence_type: splice_donor_5th_base_variant end: 30162933 feature_type: variation id: rs1347257510 seq_region_name: 22 source: dbSNP start: 30162933 strand: 1 - alleles: - G - C assembly_name: GRCh37 clinical_significance: [] consequence_type: splice_donor_region_variant end: 30162934 feature_type: variation id: rs111841046 seq_region_name: 22 source: dbSNP start: 30162934 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: splice_donor_variant end: 30162936 feature_type: variation id: rs113751462 seq_region_name: 22 source: dbSNP start: 30162936 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: splice_region_variant end: 30162938 feature_type: variation id: rs1160474064 seq_region_name: 22 source: dbSNP start: 30162938 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: splice_region_variant end: 30162939 feature_type: variation id: rs2068220605 seq_region_name: 22 source: dbSNP start: 30162939 strand: 1 - alleles: - G - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162941 feature_type: variation id: rs76121038 seq_region_name: 22 source: dbSNP start: 30162941 strand: 1 - alleles: - C - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162944 feature_type: variation id: rs988936238 seq_region_name: 22 source: dbSNP start: 30162944 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162945 feature_type: variation id: rs2068220733 seq_region_name: 22 source: dbSNP start: 30162945 strand: 1 - alleles: - C - A assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162946 feature_type: variation id: rs868299335 seq_region_name: 22 source: dbSNP start: 30162946 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162947 feature_type: variation id: rs1475885363 seq_region_name: 22 source: dbSNP start: 30162947 strand: 1 - alleles: - G - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162948 feature_type: variation id: rs1257875200 seq_region_name: 22 source: dbSNP start: 30162948 strand: 1 - alleles: - G - C assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162949 feature_type: variation id: rs947111133 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 end: 30162950 feature_type: variation id: rs2068220878 seq_region_name: 22 source: dbSNP start: 30162950 strand: 1 - alleles: - G - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162951 feature_type: variation id: rs575802940 seq_region_name: 22 source: dbSNP start: 30162951 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162954 feature_type: variation id: rs892093294 seq_region_name: 22 source: dbSNP start: 30162954 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162955 feature_type: variation id: rs2068220999 seq_region_name: 22 source: dbSNP start: 30162955 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162957 feature_type: variation id: rs2147243987 seq_region_name: 22 source: dbSNP start: 30162957 strand: 1 - alleles: - G - C assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162958 feature_type: variation id: rs933286167 seq_region_name: 22 source: dbSNP start: 30162958 strand: 1 - alleles: - C - A assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162959 feature_type: variation id: rs1052112704 seq_region_name: 22 source: dbSNP start: 30162959 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162961 feature_type: variation id: rs1328450356 seq_region_name: 22 source: dbSNP start: 30162961 strand: 1 - alleles: - G - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162963 feature_type: variation id: rs1309773191 seq_region_name: 22 source: dbSNP start: 30162963 strand: 1 - alleles: - G - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162964 feature_type: variation id: rs545944946 seq_region_name: 22 source: dbSNP start: 30162964 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162965 feature_type: variation id: rs888978022 seq_region_name: 22 source: dbSNP start: 30162965 strand: 1 - alleles: - C - A assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162966 feature_type: variation id: rs1312294475 seq_region_name: 22 source: dbSNP start: 30162966 strand: 1 - alleles: - CTCCTCCTCCTGCGTCCTC - CTCCTCCTCCTGCGTCCTCCTCCTCCTGCGTCCTC assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162984 feature_type: variation id: rs2068221261 seq_region_name: 22 source: dbSNP start: 30162966 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30162967 feature_type: variation id: rs1159663901 seq_region_name: 22 source: dbSNP start: 30162967 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: non_coding_transcript_exon_variant end: 30162970 feature_type: variation id: rs1394443565 seq_region_name: 22 source: dbSNP start: 30162970 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: non_coding_transcript_exon_variant end: 30162973 feature_type: variation id: rs2068221325 seq_region_name: 22 source: dbSNP start: 30162973 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: non_coding_transcript_exon_variant end: 30162974 feature_type: variation id: rs2068221355 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 end: 30162980 feature_type: variation id: rs1360236922 seq_region_name: 22 source: dbSNP start: 30162980 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: non_coding_transcript_exon_variant end: 30162981 feature_type: variation id: rs921570914 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 end: 30162983 feature_type: variation id: rs2068221444 seq_region_name: 22 source: dbSNP start: 30162983 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: non_coding_transcript_exon_variant end: 30162987 feature_type: variation id: rs2068221475 seq_region_name: 22 source: dbSNP start: 30162987 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: non_coding_transcript_exon_variant end: 30162991 feature_type: variation id: rs2068221505 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 end: 30162995 feature_type: variation id: rs2068221534 seq_region_name: 22 source: dbSNP start: 30162995 strand: 1 - alleles: - G - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: regulatory_region_variant end: 30163001 feature_type: variation id: rs2068221568 seq_region_name: 22 source: dbSNP start: 30163001 strand: 1 - alleles: - C - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: regulatory_region_variant end: 30163002 feature_type: variation id: rs2068221606 seq_region_name: 22 source: dbSNP start: 30163002 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: regulatory_region_variant end: 30163003 feature_type: variation id: rs766432607 seq_region_name: 22 source: dbSNP start: 30163003 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: regulatory_region_variant end: 30163004 feature_type: variation id: rs2068221665 seq_region_name: 22 source: dbSNP start: 30163004 strand: 1 - alleles: - G - C assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163014 feature_type: variation 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 end: 30163018 feature_type: variation 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 end: 30163019 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 end: 30163026 feature_type: variation 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 end: 30163031 feature_type: variation id: rs933002922 seq_region_name: 22 source: dbSNP start: 30163031 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: regulatory_region_variant end: 30163043 feature_type: variation id: rs1966795134 seq_region_name: 22 source: dbSNP start: 30163043 strand: 1 - alleles: - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: regulatory_region_variant end: 30163045 feature_type: variation id: rs1569343561 seq_region_name: 22 source: dbSNP start: 30163045 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: regulatory_region_variant end: 30163048 feature_type: variation id: rs1430434571 seq_region_name: 22 source: dbSNP start: 30163048 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: regulatory_region_variant end: 30163050 feature_type: variation 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 feature_type: variation 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 end: 30163054 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 end: 30163056 feature_type: variation 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 end: 30163057 feature_type: variation 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 end: 30163065 feature_type: variation id: rs2068222067 seq_region_name: 22 source: dbSNP start: 30163065 strand: 1 - alleles: - C - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: regulatory_region_variant end: 30163066 feature_type: variation 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 feature_type: variation id: rs1337171648 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 feature_type: variation id: rs995550641 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 feature_type: variation id: rs899028909 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 start: 30163079 strand: 1 - alleles: - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163080 feature_type: variation id: rs2068222506 seq_region_name: 22 source: dbSNP start: 30163080 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163084 feature_type: variation id: rs2068222536 seq_region_name: 22 source: dbSNP start: 30163084 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163085 feature_type: variation id: rs2068222567 seq_region_name: 22 source: dbSNP start: 30163085 strand: 1 - alleles: - GGGG - GGGGG assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163088 feature_type: variation id: rs2068222599 seq_region_name: 22 source: dbSNP start: 30163085 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163088 feature_type: variation id: rs951354833 seq_region_name: 22 source: dbSNP start: 30163088 strand: 1 - alleles: - AGAAG - AG assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163093 feature_type: variation id: rs2068222648 seq_region_name: 22 source: dbSNP start: 30163089 strand: 1 - alleles: - G - C assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163090 feature_type: variation id: rs992463585 seq_region_name: 22 source: dbSNP start: 30163090 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163092 feature_type: variation id: rs2068222716 seq_region_name: 22 source: dbSNP start: 30163092 strand: 1 - alleles: - T - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163095 feature_type: variation id: rs2068222754 seq_region_name: 22 source: dbSNP start: 30163095 strand: 1 - alleles: - G - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163099 feature_type: variation id: rs1328520047 seq_region_name: 22 source: dbSNP start: 30163099 strand: 1 - alleles: - C - A assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163101 feature_type: variation id: rs1442201910 seq_region_name: 22 source: dbSNP start: 30163101 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163104 feature_type: variation id: rs2068222861 seq_region_name: 22 source: dbSNP start: 30163104 strand: 1 - alleles: - CGA - CGACGA assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163107 feature_type: variation id: rs2068222882 seq_region_name: 22 source: dbSNP start: 30163105 strand: 1 - alleles: - G - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163110 feature_type: variation id: rs16988011 seq_region_name: 22 source: dbSNP start: 30163110 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163112 feature_type: variation id: rs1292392012 seq_region_name: 22 source: dbSNP start: 30163112 strand: 1 - alleles: - GGAG - GGAGGAG assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163120 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 end: 30163118 feature_type: variation id: rs2068222968 seq_region_name: 22 source: dbSNP start: 30163118 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163122 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 end: 30163130 feature_type: variation id: rs117507882 seq_region_name: 22 source: dbSNP start: 30163130 strand: 1 - alleles: - A - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163133 feature_type: variation id: rs981360501 seq_region_name: 22 source: dbSNP start: 30163133 strand: 1 - alleles: - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163135 feature_type: variation id: rs2068223148 seq_region_name: 22 source: dbSNP start: 30163135 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163136 feature_type: variation id: rs925432529 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 end: 30163138 feature_type: variation id: rs1195447322 seq_region_name: 22 source: dbSNP start: 30163138 strand: 1 - alleles: - T - A assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163139 feature_type: variation id: rs528669423 seq_region_name: 22 source: dbSNP start: 30163139 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163144 feature_type: variation id: rs2068223252 seq_region_name: 22 source: dbSNP start: 30163144 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163145 feature_type: variation id: rs2068223279 seq_region_name: 22 source: dbSNP start: 30163145 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163146 feature_type: variation id: rs16988015 seq_region_name: 22 source: dbSNP start: 30163146 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: regulatory_region_variant end: 30163147 feature_type: variation id: rs2068223364 seq_region_name: 22 source: dbSNP start: 30163147 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: regulatory_region_variant end: 30163148 feature_type: variation id: rs1481650735 seq_region_name: 22 source: dbSNP start: 30163148 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: regulatory_region_variant end: 30163149 feature_type: variation id: rs1265271769 seq_region_name: 22 source: dbSNP start: 30163149 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: regulatory_region_variant end: 30163156 feature_type: variation id: rs2068223450 seq_region_name: 22 source: dbSNP start: 30163156 strand: 1 - alleles: - GG - G assembly_name: GRCh37 clinical_significance: [] consequence_type: regulatory_region_variant end: 30163157 feature_type: variation id: rs2068223476 seq_region_name: 22 source: dbSNP start: 30163156 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: regulatory_region_variant end: 30163157 feature_type: variation id: rs2068223511 seq_region_name: 22 source: dbSNP start: 30163157 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: regulatory_region_variant end: 30163158 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 end: 30163164 feature_type: variation id: rs2068223566 seq_region_name: 22 source: dbSNP start: 30163158 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163163 feature_type: variation id: rs2068223602 seq_region_name: 22 source: dbSNP start: 30163163 strand: 1 - alleles: - AAAAA - AAAAAA assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163167 feature_type: variation id: rs968931161 seq_region_name: 22 source: dbSNP start: 30163163 strand: 1 - alleles: - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163165 feature_type: variation id: rs1179473019 seq_region_name: 22 source: dbSNP start: 30163165 strand: 1 - alleles: - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163166 feature_type: variation id: rs1204616528 seq_region_name: 22 source: dbSNP start: 30163166 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163167 feature_type: variation id: rs2068223846 seq_region_name: 22 source: dbSNP start: 30163167 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163168 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 end: 30163169 feature_type: variation id: rs1380123300 seq_region_name: 22 source: dbSNP start: 30163168 strand: 1 - alleles: - T - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163169 feature_type: variation id: rs913608642 seq_region_name: 22 source: dbSNP start: 30163169 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163172 feature_type: variation id: rs1438223432 seq_region_name: 22 source: dbSNP start: 30163172 strand: 1 - alleles: - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163174 feature_type: variation id: rs1299809998 seq_region_name: 22 source: dbSNP start: 30163174 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163175 feature_type: variation id: rs2068224174 seq_region_name: 22 source: dbSNP start: 30163175 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163180 feature_type: variation id: rs2068224234 seq_region_name: 22 source: dbSNP start: 30163180 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163181 feature_type: variation id: rs531877341 seq_region_name: 22 source: dbSNP start: 30163181 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163182 feature_type: variation id: rs2068224337 seq_region_name: 22 source: dbSNP start: 30163182 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163184 feature_type: variation id: rs181843365 seq_region_name: 22 source: dbSNP start: 30163184 strand: 1 - alleles: - T - A - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163185 feature_type: variation id: rs921708091 seq_region_name: 22 source: dbSNP start: 30163185 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: regulatory_region_variant end: 30163190 feature_type: variation id: rs2147244235 seq_region_name: 22 source: dbSNP start: 30163190 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: regulatory_region_variant end: 30163193 feature_type: variation id: rs1308277212 seq_region_name: 22 source: dbSNP start: 30163193 strand: 1 - alleles: - C - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: regulatory_region_variant end: 30163194 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 end: 30163196 feature_type: variation id: rs1051714805 seq_region_name: 22 source: dbSNP start: 30163196 strand: 1 - alleles: - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: regulatory_region_variant end: 30163197 feature_type: variation id: rs2068224538 seq_region_name: 22 source: dbSNP start: 30163197 strand: 1 - alleles: - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: regulatory_region_variant end: 30163198 feature_type: variation id: rs2068224576 seq_region_name: 22 source: dbSNP start: 30163198 strand: 1 - alleles: - C - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: regulatory_region_variant end: 30163199 feature_type: variation id: rs907566020 seq_region_name: 22 source: dbSNP start: 30163199 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163200 feature_type: variation 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 id: rs2068224667 seq_region_name: 22 source: dbSNP start: 30163203 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163204 feature_type: variation id: rs2068224696 seq_region_name: 22 source: dbSNP start: 30163204 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163205 feature_type: variation id: rs2068224729 seq_region_name: 22 source: dbSNP start: 30163205 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163208 feature_type: variation id: rs1377057932 seq_region_name: 22 source: dbSNP start: 30163208 strand: 1 - alleles: - T - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163210 feature_type: variation 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 feature_type: variation 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 feature_type: variation 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 feature_type: variation 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 id: rs1695298286 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 id: rs1254772821 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: [] consequence_type: TF_binding_site_variant end: 30163251 feature_type: variation id: rs2068225308 seq_region_name: 22 source: dbSNP start: 30163251 strand: 1 - alleles: - C - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163252 feature_type: variation id: rs185654343 seq_region_name: 22 source: dbSNP start: 30163252 strand: 1 - alleles: - CC - C assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163253 feature_type: variation id: rs2147244343 seq_region_name: 22 source: dbSNP start: 30163252 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163257 feature_type: variation id: rs1044841295 seq_region_name: 22 source: dbSNP start: 30163257 strand: 1 - alleles: - G - C assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163259 feature_type: variation id: rs1321051077 seq_region_name: 22 source: dbSNP start: 30163259 strand: 1 - alleles: - GG - G assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163260 feature_type: variation id: rs1170754279 seq_region_name: 22 source: dbSNP start: 30163259 strand: 1 - alleles: - T - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163262 feature_type: variation id: rs1455235860 seq_region_name: 22 source: dbSNP start: 30163262 strand: 1 - alleles: - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163265 feature_type: variation id: rs2147244361 seq_region_name: 22 source: dbSNP start: 30163265 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163268 feature_type: variation id: rs1242458411 seq_region_name: 22 source: dbSNP start: 30163268 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163269 feature_type: variation id: rs905939626 seq_region_name: 22 source: dbSNP start: 30163269 strand: 1 - alleles: - C - A - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163270 feature_type: variation id: rs146267935 seq_region_name: 22 source: dbSNP start: 30163270 strand: 1 - alleles: - G - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163274 feature_type: variation id: rs1471646245 seq_region_name: 22 source: dbSNP start: 30163274 strand: 1 - alleles: - "-" - T assembly_name: GRCh37 clinical_significance: [] consequence_type: regulatory_region_variant end: 30163274 feature_type: variation id: rs2068225631 seq_region_name: 22 source: dbSNP start: 30163275 strand: 1 - alleles: - G - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163275 feature_type: variation id: rs1199584659 seq_region_name: 22 source: dbSNP start: 30163275 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163277 feature_type: variation id: rs2068225726 seq_region_name: 22 source: dbSNP start: 30163277 strand: 1 - alleles: - A - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163279 feature_type: variation id: rs1442222300 seq_region_name: 22 source: dbSNP start: 30163279 strand: 1 - alleles: - G - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163280 feature_type: variation id: rs1254453005 seq_region_name: 22 source: dbSNP start: 30163280 strand: 1 - alleles: - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163281 feature_type: variation id: rs867508167 seq_region_name: 22 source: dbSNP start: 30163281 strand: 1 - alleles: - TT - T assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163283 feature_type: variation id: rs1268029628 seq_region_name: 22 source: dbSNP start: 30163282 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163293 feature_type: variation id: rs188846870 seq_region_name: 22 source: dbSNP start: 30163293 strand: 1 - alleles: - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163296 feature_type: variation id: rs891809822 seq_region_name: 22 source: dbSNP start: 30163296 strand: 1 - alleles: - C - A assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163302 feature_type: variation id: rs2147244404 seq_region_name: 22 source: dbSNP start: 30163302 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163303 feature_type: variation id: rs2068225944 seq_region_name: 22 source: dbSNP start: 30163303 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163304 feature_type: variation id: rs2068225976 seq_region_name: 22 source: dbSNP start: 30163304 strand: 1 - alleles: - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163305 feature_type: variation id: rs1183971160 seq_region_name: 22 source: dbSNP start: 30163305 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163307 feature_type: variation id: rs2068226035 seq_region_name: 22 source: dbSNP start: 30163307 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163308 feature_type: variation id: rs2068226063 seq_region_name: 22 source: dbSNP start: 30163308 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163309 feature_type: variation id: rs1010419172 seq_region_name: 22 source: dbSNP start: 30163309 strand: 1 - alleles: - G - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163310 feature_type: variation id: rs1601736598 seq_region_name: 22 source: dbSNP start: 30163310 strand: 1 - alleles: - TT - T assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163312 feature_type: variation id: rs2147244429 seq_region_name: 22 source: dbSNP start: 30163311 strand: 1 - alleles: - G - C assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163313 feature_type: variation id: rs2068226171 seq_region_name: 22 source: dbSNP start: 30163313 strand: 1 - alleles: - C - A assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163316 feature_type: variation id: rs2068226196 seq_region_name: 22 source: dbSNP start: 30163316 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163317 feature_type: variation id: rs1013993559 seq_region_name: 22 source: dbSNP start: 30163317 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163318 feature_type: variation id: rs1257255913 seq_region_name: 22 source: dbSNP start: 30163318 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163319 feature_type: variation id: rs1021833416 seq_region_name: 22 source: dbSNP start: 30163319 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163320 feature_type: variation id: rs1423764996 seq_region_name: 22 source: dbSNP start: 30163320 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163329 feature_type: variation id: rs2068226321 seq_region_name: 22 source: dbSNP start: 30163329 strand: 1 - alleles: - G - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163332 feature_type: variation id: rs140134 seq_region_name: 22 source: dbSNP start: 30163332 strand: 1 - alleles: - G - C assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163333 feature_type: variation id: rs970062588 seq_region_name: 22 source: dbSNP start: 30163333 strand: 1 - alleles: - A - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163334 feature_type: variation id: rs1374334413 seq_region_name: 22 source: dbSNP start: 30163334 strand: 1 - alleles: - C - A - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163336 feature_type: variation id: rs1319810002 seq_region_name: 22 source: dbSNP start: 30163336 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163337 feature_type: variation id: rs2068226599 seq_region_name: 22 source: dbSNP start: 30163337 strand: 1 - alleles: - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163338 feature_type: variation id: rs757186940 seq_region_name: 22 source: dbSNP start: 30163338 strand: 1 - alleles: - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163339 feature_type: variation id: rs1247295060 seq_region_name: 22 source: dbSNP start: 30163339 strand: 1 - alleles: - G - C assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163340 feature_type: variation id: rs2147244477 seq_region_name: 22 source: dbSNP start: 30163340 strand: 1 - alleles: - C - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163342 feature_type: variation id: rs781254885 seq_region_name: 22 source: dbSNP start: 30163342 strand: 1 - alleles: - C - "-" assembly_name: GRCh37 clinical_significance: [] consequence_type: regulatory_region_variant end: 30163342 feature_type: variation id: rs2068226714 seq_region_name: 22 source: dbSNP start: 30163342 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163343 feature_type: variation id: rs745754455 seq_region_name: 22 source: dbSNP start: 30163343 strand: 1 - alleles: - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163344 feature_type: variation id: rs769713284 seq_region_name: 22 source: dbSNP start: 30163344 strand: 1 - alleles: - C - A assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163345 feature_type: variation id: rs779935074 seq_region_name: 22 source: dbSNP start: 30163345 strand: 1 - alleles: - C - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163346 feature_type: variation id: rs2068226820 seq_region_name: 22 source: dbSNP start: 30163346 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163347 feature_type: variation id: rs1366585148 seq_region_name: 22 source: dbSNP start: 30163347 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163348 feature_type: variation id: rs566031625 seq_region_name: 22 source: dbSNP start: 30163348 strand: 1 - alleles: - A - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163349 feature_type: variation id: rs536270789 seq_region_name: 22 source: dbSNP start: 30163349 strand: 1 - alleles: - C - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163351 feature_type: variation id: rs1409831939 seq_region_name: 22 source: dbSNP start: 30163351 strand: 1 - alleles: - G - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163352 feature_type: variation id: rs1324801700 seq_region_name: 22 source: dbSNP start: 30163352 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163353 feature_type: variation id: rs1195843129 seq_region_name: 22 source: dbSNP start: 30163353 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: TF_binding_site_variant end: 30163355 feature_type: variation id: rs756593066 seq_region_name: 22 source: dbSNP start: 30163355 strand: 1 - alleles: - G - C assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30163360 feature_type: variation id: rs2068227119 seq_region_name: 22 source: dbSNP start: 30163360 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30163361 feature_type: variation id: rs770948111 seq_region_name: 22 source: dbSNP start: 30163361 strand: 1 - alleles: - C - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30163365 feature_type: variation id: rs1300672026 seq_region_name: 22 source: dbSNP start: 30163365 strand: 1 - alleles: - G - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30163366 feature_type: variation id: rs1369754618 seq_region_name: 22 source: dbSNP start: 30163366 strand: 1 - alleles: - C - A assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30163367 feature_type: variation id: rs777152072 seq_region_name: 22 source: dbSNP start: 30163367 strand: 1 - alleles: - G - C assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30163368 feature_type: variation id: rs372218155 seq_region_name: 22 source: dbSNP start: 30163368 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30163371 feature_type: variation id: rs1463169058 seq_region_name: 22 source: dbSNP start: 30163371 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30163372 feature_type: variation id: rs2068227310 seq_region_name: 22 source: dbSNP start: 30163372 strand: 1 - alleles: - G - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30163374 feature_type: variation id: rs1163580794 seq_region_name: 22 source: dbSNP start: 30163374 strand: 1 - alleles: - A - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30163375 feature_type: variation id: rs1337207410 seq_region_name: 22 source: dbSNP start: 30163375 strand: 1 - alleles: - C - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30163376 feature_type: variation id: rs1195095206 seq_region_name: 22 source: dbSNP start: 30163376 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30163377 feature_type: variation id: rs1569343784 seq_region_name: 22 source: dbSNP start: 30163377 strand: 1 - alleles: - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30163378 feature_type: variation 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 end: 30163380 feature_type: variation id: rs1290534292 seq_region_name: 22 source: dbSNP start: 30163380 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30163382 feature_type: variation id: rs765602001 seq_region_name: 22 source: dbSNP start: 30163382 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30163383 feature_type: variation id: rs2147244535 seq_region_name: 22 source: dbSNP start: 30163383 strand: 1 - alleles: - A - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30163384 feature_type: variation id: rs374440434 seq_region_name: 22 source: dbSNP start: 30163384 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30163385 feature_type: variation id: rs1229426437 seq_region_name: 22 source: dbSNP start: 30163385 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: 5_prime_UTR_variant end: 30163386 feature_type: variation id: rs368705011 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 end: 30163387 feature_type: variation id: rs375020636 seq_region_name: 22 source: dbSNP start: 30163387 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: start_lost end: 30163388 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 end: 30163390 feature_type: variation id: rs2068227623 seq_region_name: 22 source: dbSNP start: 30163390 strand: 1 - alleles: - C - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: missense_variant end: 30163392 feature_type: variation id: rs1190765049 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 end: 30163528 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 end: 30163530 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 end: 30163531 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 end: 30163534 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 end: 30163538 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 end: 30163542 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 end: 30163563 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 end: 30163576 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 end: 30163578 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 end: 30163579 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 end: 30163683 feature_type: variation id: rs1431031578 seq_region_name: 22 source: dbSNP start: 30163683 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163685 feature_type: variation id: rs745674736 seq_region_name: 22 source: dbSNP start: 30163685 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163689 feature_type: variation id: rs1966897842 seq_region_name: 22 source: dbSNP start: 30163689 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163693 feature_type: variation id: rs1209202403 seq_region_name: 22 source: dbSNP start: 30163693 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163694 feature_type: variation id: rs1160273046 seq_region_name: 22 source: dbSNP start: 30163694 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163695 feature_type: variation id: rs2068233436 seq_region_name: 22 source: dbSNP start: 30163695 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163708 feature_type: variation id: rs1838399982 seq_region_name: 22 source: dbSNP start: 30163708 strand: 1 - alleles: - G - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163709 feature_type: variation id: rs2068233463 seq_region_name: 22 source: dbSNP start: 30163709 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163710 feature_type: variation id: rs2068233495 seq_region_name: 22 source: dbSNP start: 30163710 strand: 1 - alleles: - G - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163714 feature_type: variation id: rs1464521677 seq_region_name: 22 source: dbSNP start: 30163714 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163715 feature_type: variation id: rs2068233562 seq_region_name: 22 source: dbSNP start: 30163715 strand: 1 - alleles: - G - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163716 feature_type: variation id: rs2068233593 seq_region_name: 22 source: dbSNP start: 30163716 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163719 feature_type: variation id: rs534834445 seq_region_name: 22 source: dbSNP start: 30163719 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163725 feature_type: variation id: rs949508759 seq_region_name: 22 source: dbSNP start: 30163725 strand: 1 - alleles: - TTGCAGGGGTTGTAAGTATTGC - TTGC assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163756 feature_type: variation id: rs2068233669 seq_region_name: 22 source: dbSNP start: 30163735 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163737 feature_type: variation id: rs2147245008 seq_region_name: 22 source: dbSNP start: 30163737 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163738 feature_type: variation id: rs1266276553 seq_region_name: 22 source: dbSNP start: 30163738 strand: 1 - alleles: - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163739 feature_type: variation id: rs2068233700 seq_region_name: 22 source: dbSNP start: 30163739 strand: 1 - alleles: - G - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163741 feature_type: variation id: rs1360880733 seq_region_name: 22 source: dbSNP start: 30163741 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163742 feature_type: variation id: rs2068233758 seq_region_name: 22 source: dbSNP start: 30163742 strand: 1 - alleles: - "-" - TGCCACCCTACATACCCA assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163742 feature_type: variation id: rs2068233789 seq_region_name: 22 source: dbSNP start: 30163743 strand: 1 - alleles: - G - A - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163743 feature_type: variation id: rs1046469447 seq_region_name: 22 source: dbSNP start: 30163743 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163746 feature_type: variation id: rs2068233862 seq_region_name: 22 source: dbSNP start: 30163746 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163753 feature_type: variation id: rs2068233890 seq_region_name: 22 source: dbSNP start: 30163753 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163754 feature_type: variation id: rs939189572 seq_region_name: 22 source: dbSNP start: 30163754 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163755 feature_type: variation id: rs1312264143 seq_region_name: 22 source: dbSNP start: 30163755 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163756 feature_type: variation id: rs905214711 seq_region_name: 22 source: dbSNP start: 30163756 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163768 feature_type: variation id: rs2068233988 seq_region_name: 22 source: dbSNP start: 30163768 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163770 feature_type: variation id: rs1057107945 seq_region_name: 22 source: dbSNP start: 30163770 strand: 1 - alleles: - C - "-" assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163771 feature_type: variation id: rs1367714074 seq_region_name: 22 source: dbSNP start: 30163771 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163774 feature_type: variation id: rs1299009506 seq_region_name: 22 source: dbSNP start: 30163774 strand: 1 - alleles: - A - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163778 feature_type: variation id: rs769621709 seq_region_name: 22 source: dbSNP start: 30163778 strand: 1 - alleles: - C - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163779 feature_type: variation id: rs774507549 seq_region_name: 22 source: dbSNP start: 30163779 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163785 feature_type: variation id: rs1458971498 seq_region_name: 22 source: dbSNP start: 30163785 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163797 feature_type: variation id: rs1043041029 seq_region_name: 22 source: dbSNP start: 30163797 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163808 feature_type: variation id: rs1163627661 seq_region_name: 22 source: dbSNP start: 30163808 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163810 feature_type: variation id: rs1421836286 seq_region_name: 22 source: dbSNP start: 30163810 strand: 1 - alleles: - T - TT assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163811 feature_type: variation id: rs2068234287 seq_region_name: 22 source: dbSNP start: 30163811 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163816 feature_type: variation id: rs2068234310 seq_region_name: 22 source: dbSNP start: 30163816 strand: 1 - alleles: - G - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163819 feature_type: variation id: rs1391736240 seq_region_name: 22 source: dbSNP start: 30163819 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163822 feature_type: variation id: rs2068234373 seq_region_name: 22 source: dbSNP start: 30163822 strand: 1 - alleles: - G - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163825 feature_type: variation id: rs894079794 seq_region_name: 22 source: dbSNP start: 30163825 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163831 feature_type: variation id: rs1358772268 seq_region_name: 22 source: dbSNP start: 30163831 strand: 1 - alleles: - A - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163833 feature_type: variation id: rs2068234466 seq_region_name: 22 source: dbSNP start: 30163833 strand: 1 - alleles: - G - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163834 feature_type: variation id: rs1448837679 seq_region_name: 22 source: dbSNP start: 30163834 strand: 1 - alleles: - C - A - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163835 feature_type: variation id: rs140135 seq_region_name: 22 source: dbSNP start: 30163835 strand: 1 - alleles: - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163839 feature_type: variation id: rs1601737432 seq_region_name: 22 source: dbSNP start: 30163839 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163840 feature_type: variation id: rs996416463 seq_region_name: 22 source: dbSNP start: 30163840 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163847 feature_type: variation id: rs2068234659 seq_region_name: 22 source: dbSNP start: 30163847 strand: 1 - alleles: - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163851 feature_type: variation id: rs2068234682 seq_region_name: 22 source: dbSNP start: 30163851 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163852 feature_type: variation id: rs1488846111 seq_region_name: 22 source: dbSNP start: 30163852 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163853 feature_type: variation id: rs1275448661 seq_region_name: 22 source: dbSNP start: 30163853 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163855 feature_type: variation id: rs2068234788 seq_region_name: 22 source: dbSNP start: 30163855 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163858 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 id: rs1344783150 seq_region_name: 22 source: dbSNP start: 30163861 strand: 1 - alleles: - C - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163865 feature_type: variation id: rs2068234851 seq_region_name: 22 source: dbSNP start: 30163865 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163866 feature_type: variation id: rs2068234879 seq_region_name: 22 source: dbSNP start: 30163866 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163868 feature_type: variation id: rs1601737464 seq_region_name: 22 source: dbSNP start: 30163868 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163871 feature_type: variation id: rs1275743554 seq_region_name: 22 source: dbSNP start: 30163871 strand: 1 - alleles: - C - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163876 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 end: 30163877 feature_type: variation id: rs2068235047 seq_region_name: 22 source: dbSNP start: 30163877 strand: 1 - alleles: - T - C 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 - "-" 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 - G 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 - alleles: - C - G - 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 - T 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 - G 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 - A 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 - A 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 - A 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 - C 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 - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163934 feature_type: variation id: rs2068235612 seq_region_name: 22 source: dbSNP start: 30163934 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163940 feature_type: variation id: rs760707080 seq_region_name: 22 source: dbSNP start: 30163940 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163942 feature_type: variation id: rs961788518 seq_region_name: 22 source: dbSNP start: 30163942 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163945 feature_type: variation id: rs554664649 seq_region_name: 22 source: dbSNP start: 30163945 strand: 1 - alleles: - G - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163947 feature_type: variation id: rs2147245165 seq_region_name: 22 source: dbSNP start: 30163947 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163950 feature_type: variation id: rs973080921 seq_region_name: 22 source: dbSNP start: 30163950 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163956 feature_type: variation id: rs2068235731 seq_region_name: 22 source: dbSNP start: 30163956 strand: 1 - alleles: - C - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163957 feature_type: variation id: rs1189724952 seq_region_name: 22 source: dbSNP start: 30163957 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163958 feature_type: variation id: rs2068235794 seq_region_name: 22 source: dbSNP start: 30163958 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163959 feature_type: variation id: rs1027302545 seq_region_name: 22 source: dbSNP start: 30163959 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163966 feature_type: variation id: rs2068235863 seq_region_name: 22 source: dbSNP start: 30163966 strand: 1 - alleles: - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163969 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 end: 30163970 feature_type: variation id: rs2068235913 seq_region_name: 22 source: dbSNP start: 30163970 strand: 1 - alleles: - G - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163971 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 end: 30163973 feature_type: variation id: rs2068235987 seq_region_name: 22 source: dbSNP start: 30163973 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163974 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 end: 30163981 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 end: 30163983 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 end: 30163985 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 end: 30163987 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 end: 30163988 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 end: 30163989 feature_type: variation id: rs1340469339 seq_region_name: 22 source: dbSNP start: 30163989 strand: 1 - alleles: - G - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30163990 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 end: 30163994 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 end: 30163996 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 end: 30163999 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 end: 30164005 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 end: 30164007 feature_type: variation id: rs949896213 seq_region_name: 22 source: dbSNP start: 30164007 strand: 1 - alleles: - T - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164011 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: [] consequence_type: intron_variant 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 end: 30164019 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 end: 30164024 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 end: 30164030 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 end: 30164032 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 end: 30164033 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 end: 30164035 feature_type: variation id: rs2068236526 seq_region_name: 22 source: dbSNP start: 30164035 strand: 1 - alleles: - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164040 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 end: 30164043 feature_type: variation id: rs1408995139 seq_region_name: 22 source: dbSNP start: 30164043 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164048 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 end: 30164057 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 assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164209 feature_type: variation id: rs374402521 seq_region_name: 22 source: dbSNP start: 30164209 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164211 feature_type: variation id: rs890644409 seq_region_name: 22 source: dbSNP start: 30164211 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164212 feature_type: variation id: rs1334598437 seq_region_name: 22 source: dbSNP start: 30164212 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164213 feature_type: variation id: rs2068237964 seq_region_name: 22 source: dbSNP start: 30164213 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164214 feature_type: variation id: rs2068238002 seq_region_name: 22 source: dbSNP start: 30164214 strand: 1 - alleles: - A - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164217 feature_type: variation id: rs185333042 seq_region_name: 22 source: dbSNP start: 30164217 strand: 1 - alleles: - C - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164218 feature_type: variation id: rs2068238071 seq_region_name: 22 source: dbSNP start: 30164218 strand: 1 - alleles: - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164220 feature_type: variation id: rs1389391284 seq_region_name: 22 source: dbSNP start: 30164220 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164221 feature_type: variation id: rs1229347660 seq_region_name: 22 source: dbSNP start: 30164221 strand: 1 - alleles: - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164228 feature_type: variation id: rs2068238132 seq_region_name: 22 source: dbSNP start: 30164228 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164233 feature_type: variation id: rs1288592165 seq_region_name: 22 source: dbSNP start: 30164233 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164235 feature_type: variation id: rs1319372704 seq_region_name: 22 source: dbSNP start: 30164235 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164237 feature_type: variation id: rs2068238199 seq_region_name: 22 source: dbSNP start: 30164237 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164238 feature_type: variation id: rs2068238226 seq_region_name: 22 source: dbSNP start: 30164238 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164241 feature_type: variation id: rs2068238259 seq_region_name: 22 source: dbSNP start: 30164241 strand: 1 - alleles: - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164243 feature_type: variation id: rs1018163707 seq_region_name: 22 source: dbSNP start: 30164243 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164244 feature_type: variation id: rs2068238314 seq_region_name: 22 source: dbSNP start: 30164244 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164247 feature_type: variation id: rs2068238341 seq_region_name: 22 source: dbSNP start: 30164247 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164251 feature_type: variation id: rs2068238368 seq_region_name: 22 source: dbSNP start: 30164251 strand: 1 - alleles: - G - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164254 feature_type: variation id: rs2068238394 seq_region_name: 22 source: dbSNP start: 30164254 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164255 feature_type: variation id: rs1370397639 seq_region_name: 22 source: dbSNP start: 30164255 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164257 feature_type: variation id: rs890704701 seq_region_name: 22 source: dbSNP start: 30164257 strand: 1 - alleles: - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164261 feature_type: variation id: rs2068238485 seq_region_name: 22 source: dbSNP start: 30164261 strand: 1 - alleles: - G - "-" assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164264 feature_type: variation id: rs1200211464 seq_region_name: 22 source: dbSNP start: 30164264 strand: 1 - alleles: - AGGTAGGAATCGCAACACA - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164287 feature_type: variation id: rs1254692040 seq_region_name: 22 source: dbSNP start: 30164269 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164276 feature_type: variation id: rs1601737707 seq_region_name: 22 source: dbSNP start: 30164276 strand: 1 - alleles: - C - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164279 feature_type: variation id: rs1211063927 seq_region_name: 22 source: dbSNP start: 30164279 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164280 feature_type: variation id: rs2068238616 seq_region_name: 22 source: dbSNP start: 30164280 strand: 1 - alleles: - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164287 feature_type: variation id: rs115595018 seq_region_name: 22 source: dbSNP start: 30164287 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164288 feature_type: variation id: rs1036514169 seq_region_name: 22 source: dbSNP start: 30164288 strand: 1 - alleles: - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164293 feature_type: variation id: rs139348486 seq_region_name: 22 source: dbSNP start: 30164293 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164295 feature_type: variation id: rs569761080 seq_region_name: 22 source: dbSNP start: 30164295 strand: 1 - alleles: - TTTT - TT assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164299 feature_type: variation id: rs375549411 seq_region_name: 22 source: dbSNP start: 30164296 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164298 feature_type: variation id: rs2068238770 seq_region_name: 22 source: dbSNP start: 30164298 strand: 1 - alleles: - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164300 feature_type: variation id: rs2068238797 seq_region_name: 22 source: dbSNP start: 30164300 strand: 1 - alleles: - A - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164311 feature_type: variation id: rs184101675 seq_region_name: 22 source: dbSNP start: 30164311 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164321 feature_type: variation id: rs950356122 seq_region_name: 22 source: dbSNP start: 30164321 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164327 feature_type: variation id: rs2068238877 seq_region_name: 22 source: dbSNP start: 30164327 strand: 1 - alleles: - A - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164330 feature_type: variation id: rs1732703264 seq_region_name: 22 source: dbSNP start: 30164330 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164331 feature_type: variation id: rs2068238910 seq_region_name: 22 source: dbSNP start: 30164331 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164339 feature_type: variation id: rs1238946565 seq_region_name: 22 source: dbSNP start: 30164339 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164341 feature_type: variation id: rs1245327843 seq_region_name: 22 source: dbSNP start: 30164341 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164342 feature_type: variation id: rs2068239000 seq_region_name: 22 source: dbSNP start: 30164342 strand: 1 - alleles: - T - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164344 feature_type: variation id: rs2147245435 seq_region_name: 22 source: dbSNP start: 30164344 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164350 feature_type: variation id: rs994572627 seq_region_name: 22 source: dbSNP start: 30164350 strand: 1 - alleles: - TGTG - TG assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164358 feature_type: variation id: rs2068239060 seq_region_name: 22 source: dbSNP start: 30164355 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164356 feature_type: variation id: rs2068239092 seq_region_name: 22 source: dbSNP start: 30164356 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164359 feature_type: variation id: rs1027819295 seq_region_name: 22 source: dbSNP start: 30164359 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164361 feature_type: variation id: rs2147245442 seq_region_name: 22 source: dbSNP start: 30164361 strand: 1 - alleles: - C - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164369 feature_type: variation id: rs16988025 seq_region_name: 22 source: dbSNP start: 30164369 strand: 1 - alleles: - A - AA assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164373 feature_type: variation id: rs1389503549 seq_region_name: 22 source: dbSNP start: 30164373 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164374 feature_type: variation id: rs755355164 seq_region_name: 22 source: dbSNP start: 30164374 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164376 feature_type: variation id: rs1320034731 seq_region_name: 22 source: dbSNP start: 30164376 strand: 1 - alleles: - T - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164378 feature_type: variation id: rs1024211284 seq_region_name: 22 source: dbSNP start: 30164378 strand: 1 - alleles: - A - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164379 feature_type: variation id: rs971691894 seq_region_name: 22 source: dbSNP start: 30164379 strand: 1 - alleles: - T - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164380 feature_type: variation id: rs570589614 seq_region_name: 22 source: dbSNP start: 30164380 strand: 1 - alleles: - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164381 feature_type: variation id: rs1172837002 seq_region_name: 22 source: dbSNP start: 30164381 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164384 feature_type: variation id: rs1401309771 seq_region_name: 22 source: dbSNP start: 30164384 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164387 feature_type: variation id: rs774998073 seq_region_name: 22 source: dbSNP start: 30164387 strand: 1 - alleles: - C - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164390 feature_type: variation id: rs2068239505 seq_region_name: 22 source: dbSNP start: 30164390 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164391 feature_type: variation id: rs1383720752 seq_region_name: 22 source: dbSNP start: 30164391 strand: 1 - alleles: - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164399 feature_type: variation id: rs2068239540 seq_region_name: 22 source: dbSNP start: 30164399 strand: 1 - alleles: - ACTT - "-" assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164402 feature_type: variation id: rs1446278618 seq_region_name: 22 source: dbSNP start: 30164399 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164401 feature_type: variation id: rs2068239598 seq_region_name: 22 source: dbSNP start: 30164401 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164402 feature_type: variation id: rs2068239627 seq_region_name: 22 source: dbSNP start: 30164402 strand: 1 - alleles: - T - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164407 feature_type: variation id: rs1450682337 seq_region_name: 22 source: dbSNP start: 30164407 strand: 1 - alleles: - TTTAATTT - TTT assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164415 feature_type: variation id: rs2068239681 seq_region_name: 22 source: dbSNP start: 30164408 strand: 1 - alleles: - G - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164416 feature_type: variation id: rs2068239714 seq_region_name: 22 source: dbSNP start: 30164416 strand: 1 - alleles: - CTGTCTG - CTG assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164426 feature_type: variation id: rs2068239742 seq_region_name: 22 source: dbSNP start: 30164420 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164421 feature_type: variation id: rs2068239778 seq_region_name: 22 source: dbSNP start: 30164421 strand: 1 - alleles: - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164422 feature_type: variation id: rs2068239820 seq_region_name: 22 source: dbSNP start: 30164422 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164423 feature_type: variation id: rs960591060 seq_region_name: 22 source: dbSNP start: 30164423 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164426 feature_type: variation id: rs2068239877 seq_region_name: 22 source: dbSNP start: 30164426 strand: 1 - alleles: - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164427 feature_type: variation id: rs1601737790 seq_region_name: 22 source: dbSNP start: 30164427 strand: 1 - alleles: - CTCT - CT assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164431 feature_type: variation id: rs2068239948 seq_region_name: 22 source: dbSNP start: 30164428 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164432 feature_type: variation id: rs765629817 seq_region_name: 22 source: dbSNP start: 30164432 strand: 1 - alleles: - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164435 feature_type: variation id: rs1444775906 seq_region_name: 22 source: dbSNP start: 30164435 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164436 feature_type: variation id: rs1342615878 seq_region_name: 22 source: dbSNP start: 30164436 strand: 1 - alleles: - C - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164438 feature_type: variation id: rs988044453 seq_region_name: 22 source: dbSNP start: 30164438 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164439 feature_type: variation id: rs534537269 seq_region_name: 22 source: dbSNP start: 30164439 strand: 1 - alleles: - A - 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 id: rs1681619766 seq_region_name: 22 source: dbSNP start: 30164443 strand: 1 - alleles: - G - A 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: - C - 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 id: rs978831357 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 - alleles: - T - "-" assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164464 feature_type: variation id: rs1365917132 seq_region_name: 22 source: dbSNP start: 30164464 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164464 feature_type: variation id: rs2068240345 seq_region_name: 22 source: dbSNP start: 30164464 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164468 feature_type: variation id: rs2068240400 seq_region_name: 22 source: dbSNP start: 30164468 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164472 feature_type: variation id: rs1296780960 seq_region_name: 22 source: dbSNP start: 30164472 strand: 1 - alleles: - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164475 feature_type: variation id: rs2068240456 seq_region_name: 22 source: dbSNP start: 30164475 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164476 feature_type: variation id: rs752328080 seq_region_name: 22 source: dbSNP start: 30164476 strand: 1 - alleles: - CC - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164477 feature_type: variation id: rs1428733370 seq_region_name: 22 source: dbSNP start: 30164476 strand: 1 - alleles: - CCAGTGCAAC - "-" assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164485 feature_type: variation id: rs1332849327 seq_region_name: 22 source: dbSNP start: 30164476 strand: 1 - alleles: - G - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164479 feature_type: variation id: rs144094912 seq_region_name: 22 source: dbSNP start: 30164479 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164485 feature_type: variation id: rs2147245578 seq_region_name: 22 source: dbSNP start: 30164485 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164491 feature_type: variation id: rs2068240589 seq_region_name: 22 source: dbSNP start: 30164491 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164499 feature_type: variation id: rs2068240623 seq_region_name: 22 source: dbSNP start: 30164499 strand: 1 - alleles: - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164504 feature_type: variation id: rs2068240657 seq_region_name: 22 source: dbSNP start: 30164504 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164505 feature_type: variation id: rs1363913728 seq_region_name: 22 source: dbSNP start: 30164505 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164506 feature_type: variation id: rs1170925605 seq_region_name: 22 source: dbSNP start: 30164506 strand: 1 - alleles: - C - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164510 feature_type: variation id: rs2147245596 seq_region_name: 22 source: dbSNP start: 30164510 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164511 feature_type: variation id: rs12158466 seq_region_name: 22 source: dbSNP start: 30164511 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164512 feature_type: variation id: rs2068240771 seq_region_name: 22 source: dbSNP start: 30164512 strand: 1 - alleles: - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164515 feature_type: variation id: rs945359753 seq_region_name: 22 source: dbSNP start: 30164515 strand: 1 - alleles: - CCC - CC assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164519 feature_type: variation id: rs2068240820 seq_region_name: 22 source: dbSNP start: 30164517 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164518 feature_type: variation id: rs1166595815 seq_region_name: 22 source: dbSNP start: 30164518 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164520 feature_type: variation id: rs2068240859 seq_region_name: 22 source: dbSNP start: 30164520 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164522 feature_type: variation id: rs1601737864 seq_region_name: 22 source: dbSNP start: 30164522 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164524 feature_type: variation id: rs2068240904 seq_region_name: 22 source: dbSNP start: 30164524 strand: 1 - alleles: - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164527 feature_type: variation id: rs1474146233 seq_region_name: 22 source: dbSNP start: 30164527 strand: 1 - alleles: - C - A - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164528 feature_type: variation id: rs1258062595 seq_region_name: 22 source: dbSNP start: 30164528 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164529 feature_type: variation id: rs1316954163 seq_region_name: 22 source: dbSNP start: 30164529 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164530 feature_type: variation id: rs1043062528 seq_region_name: 22 source: dbSNP start: 30164530 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164533 feature_type: variation id: rs574577222 seq_region_name: 22 source: dbSNP start: 30164533 strand: 1 - alleles: - G - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164539 feature_type: variation id: rs2068241100 seq_region_name: 22 source: dbSNP start: 30164539 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164548 feature_type: variation id: rs2068241127 seq_region_name: 22 source: dbSNP start: 30164548 strand: 1 - alleles: - C - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164550 feature_type: variation id: rs186630137 seq_region_name: 22 source: dbSNP start: 30164550 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164553 feature_type: variation id: rs2068241197 seq_region_name: 22 source: dbSNP start: 30164553 strand: 1 - alleles: - TGATCTG - TG assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164560 feature_type: variation id: rs1442755618 seq_region_name: 22 source: dbSNP start: 30164554 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164560 feature_type: variation id: rs746546572 seq_region_name: 22 source: dbSNP start: 30164560 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164565 feature_type: variation id: rs1266315237 seq_region_name: 22 source: dbSNP start: 30164565 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164567 feature_type: variation id: rs1601737893 seq_region_name: 22 source: dbSNP start: 30164567 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164570 feature_type: variation id: rs2068241346 seq_region_name: 22 source: dbSNP start: 30164570 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164571 feature_type: variation id: rs763514034 seq_region_name: 22 source: dbSNP start: 30164571 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164573 feature_type: variation id: rs2068241401 seq_region_name: 22 source: dbSNP start: 30164573 strand: 1 - alleles: - T - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164577 feature_type: variation id: rs2068241437 seq_region_name: 22 source: dbSNP start: 30164577 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164579 feature_type: variation id: rs1207121255 seq_region_name: 22 source: dbSNP start: 30164579 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164582 feature_type: variation id: rs1342530582 seq_region_name: 22 source: dbSNP start: 30164582 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164584 feature_type: variation id: rs1235679537 seq_region_name: 22 source: dbSNP start: 30164584 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164590 feature_type: variation id: rs2147245671 seq_region_name: 22 source: dbSNP start: 30164590 strand: 1 - alleles: - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164591 feature_type: variation id: rs1601737899 seq_region_name: 22 source: dbSNP start: 30164591 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164593 feature_type: variation id: rs2147245679 seq_region_name: 22 source: dbSNP start: 30164593 strand: 1 - alleles: - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164595 feature_type: variation id: rs1601737902 seq_region_name: 22 source: dbSNP start: 30164595 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164597 feature_type: variation id: rs2147245689 seq_region_name: 22 source: dbSNP start: 30164597 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164600 feature_type: variation id: rs1273850790 seq_region_name: 22 source: dbSNP start: 30164600 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164601 feature_type: variation id: rs2068241599 seq_region_name: 22 source: dbSNP start: 30164601 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164602 feature_type: variation id: rs1212685409 seq_region_name: 22 source: dbSNP start: 30164602 strand: 1 - alleles: - T - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164603 feature_type: variation id: rs2068241661 seq_region_name: 22 source: dbSNP start: 30164603 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164605 feature_type: variation id: rs1347259397 seq_region_name: 22 source: dbSNP start: 30164605 strand: 1 - alleles: - G - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164606 feature_type: variation id: rs2147245699 seq_region_name: 22 source: dbSNP start: 30164606 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164607 feature_type: variation id: rs1343933238 seq_region_name: 22 source: dbSNP start: 30164607 strand: 1 - alleles: - C - "-" assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164607 feature_type: variation id: rs1478724430 seq_region_name: 22 source: dbSNP start: 30164607 strand: 1 - alleles: - TTTTTTTT - TTTT - TTTTTTT - TTTTTTTTT - TTTTTTTTTTTTTTTTTTTTTTTTT assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164615 feature_type: variation id: rs199719762 seq_region_name: 22 source: dbSNP start: 30164608 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164611 feature_type: variation id: rs2068241819 seq_region_name: 22 source: dbSNP start: 30164611 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164612 feature_type: variation id: rs897955178 seq_region_name: 22 source: dbSNP start: 30164612 strand: 1 - alleles: - TTTTGTTTTGTTTTGTTTT - TTTTGTTTTGTTTT - TTTTGTTTTGTTTTGTTTTGTTTT assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164630 feature_type: variation id: rs749024318 seq_region_name: 22 source: dbSNP start: 30164612 strand: 1 - alleles: - "-" - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164612 feature_type: variation id: rs1327457929 seq_region_name: 22 source: dbSNP start: 30164613 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164613 feature_type: variation id: rs1172717538 seq_region_name: 22 source: dbSNP start: 30164613 strand: 1 - alleles: - TTTGTTT - TTT assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164619 feature_type: variation id: rs1441575717 seq_region_name: 22 source: dbSNP start: 30164613 strand: 1 - alleles: - TTTGTTTTGTTTTGTTT - TTT assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164629 feature_type: variation id: rs2068241974 seq_region_name: 22 source: dbSNP start: 30164613 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164614 feature_type: variation id: rs556949282 seq_region_name: 22 source: dbSNP start: 30164614 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164615 feature_type: variation id: rs575323739 seq_region_name: 22 source: dbSNP start: 30164615 strand: 1 - alleles: - TG - GT assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164616 feature_type: variation id: rs386820602 seq_region_name: 22 source: dbSNP start: 30164615 strand: 1 - alleles: - TGT - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164617 feature_type: variation id: rs1426779204 seq_region_name: 22 source: dbSNP start: 30164615 strand: 1 - alleles: - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164616 feature_type: variation id: rs140136 seq_region_name: 22 source: dbSNP start: 30164616 strand: 1 - alleles: - G - "-" assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164616 feature_type: variation id: rs112759265 seq_region_name: 22 source: dbSNP start: 30164616 strand: 1 - alleles: - GT - TG assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164617 feature_type: variation id: rs386820603 seq_region_name: 22 source: dbSNP start: 30164616 strand: 1 - alleles: - GTTTTG - "-" assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164621 feature_type: variation id: rs1232052451 seq_region_name: 22 source: dbSNP start: 30164616 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164617 feature_type: variation id: rs150623347 seq_region_name: 22 source: dbSNP start: 30164617 strand: 1 - alleles: - TTTT - TTT - TTTTT assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164620 feature_type: variation id: rs1444114939 seq_region_name: 22 source: dbSNP start: 30164617 strand: 1 - alleles: - "-" - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164617 feature_type: variation id: rs904937048 seq_region_name: 22 source: dbSNP start: 30164618 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164618 feature_type: variation id: rs532870343 seq_region_name: 22 source: dbSNP start: 30164618 strand: 1 - alleles: - T - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164619 feature_type: variation id: rs1034633016 seq_region_name: 22 source: dbSNP start: 30164619 strand: 1 - alleles: - TTGTT - TT assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164623 feature_type: variation id: rs2068242458 seq_region_name: 22 source: dbSNP start: 30164619 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164620 feature_type: variation id: rs1465350009 seq_region_name: 22 source: dbSNP start: 30164620 strand: 1 - alleles: - TGT - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164622 feature_type: variation id: rs1350284462 seq_region_name: 22 source: dbSNP start: 30164620 strand: 1 - alleles: - "-" - TG assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164620 feature_type: variation id: rs2068242542 seq_region_name: 22 source: dbSNP start: 30164621 strand: 1 - alleles: - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164621 feature_type: variation id: rs12627756 seq_region_name: 22 source: dbSNP start: 30164621 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164622 feature_type: variation id: rs1468849211 seq_region_name: 22 source: dbSNP start: 30164622 strand: 1 - alleles: - TTTT - TTT - TTTTT - TTTTTT assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164625 feature_type: variation id: rs368297891 seq_region_name: 22 source: dbSNP start: 30164622 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164623 feature_type: variation id: rs1009418133 seq_region_name: 22 source: dbSNP start: 30164623 strand: 1 - alleles: - TT - TTGTT assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164624 feature_type: variation id: rs1166342820 seq_region_name: 22 source: dbSNP start: 30164623 strand: 1 - alleles: - "-" - C - GTG assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164624 feature_type: variation id: rs1020831437 seq_region_name: 22 source: dbSNP start: 30164625 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164625 feature_type: variation id: rs1476305351 seq_region_name: 22 source: dbSNP start: 30164625 strand: 1 - alleles: - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164626 feature_type: variation id: rs140137 seq_region_name: 22 source: dbSNP start: 30164626 strand: 1 - alleles: - G - "-" assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164626 feature_type: variation id: rs367821940 seq_region_name: 22 source: dbSNP start: 30164626 strand: 1 - alleles: - G - TT assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164626 feature_type: variation id: rs1556024864 seq_region_name: 22 source: dbSNP start: 30164626 strand: 1 - alleles: - GTT - TTG assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164628 feature_type: variation id: rs386820604 seq_region_name: 22 source: dbSNP start: 30164626 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164627 feature_type: variation id: rs1237989847 seq_region_name: 22 source: dbSNP start: 30164627 strand: 1 - alleles: - TTTTTTT - TTTTTTTT assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164633 feature_type: variation id: rs1175325333 seq_region_name: 22 source: dbSNP start: 30164627 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164628 feature_type: variation id: rs140138 seq_region_name: 22 source: dbSNP start: 30164628 strand: 1 - alleles: - "-" - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164628 feature_type: variation id: rs1460051274 seq_region_name: 22 source: dbSNP start: 30164629 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164629 feature_type: variation id: rs867909937 seq_region_name: 22 source: dbSNP start: 30164629 strand: 1 - alleles: - TTTTT - TTTTTTTGTTTTT assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164633 feature_type: variation id: rs2068243141 seq_region_name: 22 source: dbSNP start: 30164629 strand: 1 - alleles: - "-" - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164629 feature_type: variation id: rs199967352 seq_region_name: 22 source: dbSNP start: 30164630 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164630 feature_type: variation id: rs2068243196 seq_region_name: 22 source: dbSNP start: 30164630 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164633 feature_type: variation id: rs1316602246 seq_region_name: 22 source: dbSNP start: 30164633 strand: 1 - alleles: - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164634 feature_type: variation id: rs1374173658 seq_region_name: 22 source: dbSNP start: 30164634 strand: 1 - alleles: - A - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164637 feature_type: variation id: rs967875226 seq_region_name: 22 source: dbSNP start: 30164637 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164638 feature_type: variation id: rs944932585 seq_region_name: 22 source: dbSNP start: 30164638 strand: 1 - alleles: - C - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164644 feature_type: variation id: rs1028197933 seq_region_name: 22 source: dbSNP start: 30164644 strand: 1 - alleles: - CTCACTC - CTC assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164650 feature_type: variation id: rs1569344439 seq_region_name: 22 source: dbSNP start: 30164644 strand: 1 - alleles: - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164647 feature_type: variation id: rs2068243446 seq_region_name: 22 source: dbSNP start: 30164647 strand: 1 - alleles: - CTCT - CT assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164651 feature_type: variation id: rs1278301250 seq_region_name: 22 source: dbSNP start: 30164648 strand: 1 - alleles: - C - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164650 feature_type: variation id: rs1698314734 seq_region_name: 22 source: dbSNP start: 30164650 strand: 1 - alleles: - TGT - TGTGT assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164653 feature_type: variation id: rs2068243501 seq_region_name: 22 source: dbSNP start: 30164651 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164654 feature_type: variation id: rs2068243534 seq_region_name: 22 source: dbSNP start: 30164654 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164655 feature_type: variation id: rs1039208118 seq_region_name: 22 source: dbSNP start: 30164655 strand: 1 - alleles: - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164666 feature_type: variation id: rs1339250290 seq_region_name: 22 source: dbSNP start: 30164666 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164674 feature_type: variation id: rs1224834926 seq_region_name: 22 source: dbSNP start: 30164674 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164675 feature_type: variation id: rs2068243605 seq_region_name: 22 source: dbSNP start: 30164675 strand: 1 - alleles: - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164680 feature_type: variation id: rs1457300793 seq_region_name: 22 source: dbSNP start: 30164680 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164681 feature_type: variation id: rs1276243971 seq_region_name: 22 source: dbSNP start: 30164681 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164682 feature_type: variation id: rs2068243681 seq_region_name: 22 source: dbSNP start: 30164682 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164690 feature_type: variation id: rs2068243709 seq_region_name: 22 source: dbSNP start: 30164690 strand: 1 - alleles: - G - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164693 feature_type: variation id: rs953569569 seq_region_name: 22 source: dbSNP start: 30164693 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164695 feature_type: variation id: rs2068243765 seq_region_name: 22 source: dbSNP start: 30164695 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164696 feature_type: variation id: rs2068243789 seq_region_name: 22 source: dbSNP start: 30164696 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164707 feature_type: variation id: rs2068243807 seq_region_name: 22 source: dbSNP start: 30164707 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164711 feature_type: variation id: rs1156407328 seq_region_name: 22 source: dbSNP start: 30164711 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164715 feature_type: variation id: rs1406890548 seq_region_name: 22 source: dbSNP start: 30164715 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164722 feature_type: variation id: rs530129022 seq_region_name: 22 source: dbSNP start: 30164722 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164725 feature_type: variation id: rs2068243924 seq_region_name: 22 source: dbSNP start: 30164725 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164726 feature_type: variation id: rs986261764 seq_region_name: 22 source: dbSNP start: 30164726 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164729 feature_type: variation id: rs1442743704 seq_region_name: 22 source: dbSNP start: 30164729 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164730 feature_type: variation id: rs1249789414 seq_region_name: 22 source: dbSNP start: 30164730 strand: 1 - alleles: - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164734 feature_type: variation id: rs2068244035 seq_region_name: 22 source: dbSNP start: 30164734 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164735 feature_type: variation id: rs1345217133 seq_region_name: 22 source: dbSNP start: 30164735 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164736 feature_type: variation id: rs2068244101 seq_region_name: 22 source: dbSNP start: 30164736 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164738 feature_type: variation id: rs1199667791 seq_region_name: 22 source: dbSNP start: 30164738 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164739 feature_type: variation id: rs1485547878 seq_region_name: 22 source: dbSNP start: 30164739 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164743 feature_type: variation id: rs2068244177 seq_region_name: 22 source: dbSNP start: 30164743 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164747 feature_type: variation id: rs2068244205 seq_region_name: 22 source: dbSNP start: 30164747 strand: 1 - alleles: - T - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164748 feature_type: variation id: rs1276194479 seq_region_name: 22 source: dbSNP start: 30164748 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164749 feature_type: variation id: rs1223995171 seq_region_name: 22 source: dbSNP start: 30164749 strand: 1 - alleles: - G - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164750 feature_type: variation id: rs1322735070 seq_region_name: 22 source: dbSNP start: 30164750 strand: 1 - alleles: - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164751 feature_type: variation id: rs2068244328 seq_region_name: 22 source: dbSNP start: 30164751 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164760 feature_type: variation id: rs2068244364 seq_region_name: 22 source: dbSNP start: 30164760 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164765 feature_type: variation id: rs139520152 seq_region_name: 22 source: dbSNP start: 30164765 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164769 feature_type: variation id: rs1244213707 seq_region_name: 22 source: dbSNP start: 30164769 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164772 feature_type: variation id: rs1345014338 seq_region_name: 22 source: dbSNP start: 30164772 strand: 1 - alleles: - G - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164773 feature_type: variation id: rs563301528 seq_region_name: 22 source: dbSNP start: 30164773 strand: 1 - alleles: - G - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164797 feature_type: variation id: rs377101531 seq_region_name: 22 source: dbSNP start: 30164797 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164804 feature_type: variation id: rs2068244471 seq_region_name: 22 source: dbSNP start: 30164804 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164807 feature_type: variation id: rs2068244493 seq_region_name: 22 source: dbSNP start: 30164807 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164815 feature_type: variation id: rs972274843 seq_region_name: 22 source: dbSNP start: 30164815 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164816 feature_type: variation id: rs2068244554 seq_region_name: 22 source: dbSNP start: 30164816 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164820 feature_type: variation id: rs2068244583 seq_region_name: 22 source: dbSNP start: 30164820 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164827 feature_type: variation id: rs1360590682 seq_region_name: 22 source: dbSNP start: 30164827 strand: 1 - alleles: - C - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164828 feature_type: variation id: rs552417714 seq_region_name: 22 source: dbSNP start: 30164828 strand: 1 - alleles: - T - "-" assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164829 feature_type: variation id: rs2068244647 seq_region_name: 22 source: dbSNP start: 30164829 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164843 feature_type: variation id: rs570642224 seq_region_name: 22 source: dbSNP start: 30164843 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164844 feature_type: variation id: rs2068244702 seq_region_name: 22 source: dbSNP start: 30164844 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164849 feature_type: variation id: rs930947892 seq_region_name: 22 source: dbSNP start: 30164849 strand: 1 - alleles: - T - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164856 feature_type: variation id: rs2068244760 seq_region_name: 22 source: dbSNP start: 30164856 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164857 feature_type: variation id: rs2068244796 seq_region_name: 22 source: dbSNP start: 30164857 strand: 1 - alleles: - CTTA - CTTACTTA assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164868 feature_type: variation id: rs1350078047 seq_region_name: 22 source: dbSNP start: 30164865 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164871 feature_type: variation id: rs1162747568 seq_region_name: 22 source: dbSNP start: 30164871 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164872 feature_type: variation id: rs2100204040 seq_region_name: 22 source: dbSNP start: 30164872 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164873 feature_type: variation id: rs2068244880 seq_region_name: 22 source: dbSNP start: 30164873 strand: 1 - alleles: - C - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164874 feature_type: variation id: rs2068244899 seq_region_name: 22 source: dbSNP start: 30164874 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164882 feature_type: variation id: rs745799533 seq_region_name: 22 source: dbSNP start: 30164882 strand: 1 - alleles: - G - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164885 feature_type: variation id: rs769521932 seq_region_name: 22 source: dbSNP start: 30164885 strand: 1 - alleles: - G - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164886 feature_type: variation id: rs2147245971 seq_region_name: 22 source: dbSNP start: 30164886 strand: 1 - alleles: - C - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164891 feature_type: variation id: rs534960042 seq_region_name: 22 source: dbSNP start: 30164891 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164895 feature_type: variation id: rs1049675882 seq_region_name: 22 source: dbSNP start: 30164895 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164896 feature_type: variation id: rs534472200 seq_region_name: 22 source: dbSNP start: 30164896 strand: 1 - alleles: - GTG - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164898 feature_type: variation id: rs2068245071 seq_region_name: 22 source: dbSNP start: 30164896 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164898 feature_type: variation id: rs1379598745 seq_region_name: 22 source: dbSNP start: 30164898 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164901 feature_type: variation id: rs1428018649 seq_region_name: 22 source: dbSNP start: 30164901 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164902 feature_type: variation id: rs553851404 seq_region_name: 22 source: dbSNP start: 30164902 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164909 feature_type: variation id: rs1004565234 seq_region_name: 22 source: dbSNP start: 30164909 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164910 feature_type: variation id: rs2068245228 seq_region_name: 22 source: dbSNP start: 30164910 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164911 feature_type: variation id: rs2068245259 seq_region_name: 22 source: dbSNP start: 30164911 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164912 feature_type: variation id: rs1056163022 seq_region_name: 22 source: dbSNP start: 30164912 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164913 feature_type: variation id: rs2147246007 seq_region_name: 22 source: dbSNP start: 30164913 strand: 1 - alleles: - C - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164915 feature_type: variation id: rs568265591 seq_region_name: 22 source: dbSNP start: 30164915 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164916 feature_type: variation id: rs2068245338 seq_region_name: 22 source: dbSNP start: 30164916 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164917 feature_type: variation id: rs2068245372 seq_region_name: 22 source: dbSNP start: 30164917 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164920 feature_type: variation id: rs971341471 seq_region_name: 22 source: dbSNP start: 30164920 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164924 feature_type: variation id: rs2068245438 seq_region_name: 22 source: dbSNP start: 30164924 strand: 1 - alleles: - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164934 feature_type: variation id: rs1220808175 seq_region_name: 22 source: dbSNP start: 30164934 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164935 feature_type: variation id: rs1344674067 seq_region_name: 22 source: dbSNP start: 30164935 strand: 1 - alleles: - T - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164941 feature_type: variation id: rs2068245509 seq_region_name: 22 source: dbSNP start: 30164941 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164942 feature_type: variation id: rs1422113885 seq_region_name: 22 source: dbSNP start: 30164942 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164943 feature_type: variation id: rs1042073566 seq_region_name: 22 source: dbSNP start: 30164943 strand: 1 - alleles: - C - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164945 feature_type: variation id: rs2050543780 seq_region_name: 22 source: dbSNP start: 30164945 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164951 feature_type: variation id: rs1227272069 seq_region_name: 22 source: dbSNP start: 30164951 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164952 feature_type: variation id: rs1306441637 seq_region_name: 22 source: dbSNP start: 30164952 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164956 feature_type: variation id: rs1001821344 seq_region_name: 22 source: dbSNP start: 30164956 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164957 feature_type: variation id: rs1168937844 seq_region_name: 22 source: dbSNP start: 30164957 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164958 feature_type: variation id: rs903767655 seq_region_name: 22 source: dbSNP start: 30164958 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164965 feature_type: variation id: rs1220431976 seq_region_name: 22 source: dbSNP start: 30164965 strand: 1 - alleles: - T - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164967 feature_type: variation id: rs2147246040 seq_region_name: 22 source: dbSNP start: 30164967 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164968 feature_type: variation id: rs1345813688 seq_region_name: 22 source: dbSNP start: 30164968 strand: 1 - alleles: - G - A - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164976 feature_type: variation id: rs1034178452 seq_region_name: 22 source: dbSNP start: 30164976 strand: 1 - alleles: - T - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164978 feature_type: variation id: rs2068245797 seq_region_name: 22 source: dbSNP start: 30164978 strand: 1 - alleles: - C - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164979 feature_type: variation id: rs2068245826 seq_region_name: 22 source: dbSNP start: 30164979 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164981 feature_type: variation id: rs957197692 seq_region_name: 22 source: dbSNP start: 30164981 strand: 1 - alleles: - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164985 feature_type: variation id: rs1601738255 seq_region_name: 22 source: dbSNP start: 30164985 strand: 1 - alleles: - T - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164991 feature_type: variation id: rs2068245898 seq_region_name: 22 source: dbSNP start: 30164991 strand: 1 - alleles: - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164997 feature_type: variation id: rs2068245930 seq_region_name: 22 source: dbSNP start: 30164997 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30164999 feature_type: variation id: rs748988580 seq_region_name: 22 source: dbSNP start: 30164999 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165002 feature_type: variation id: rs1372126586 seq_region_name: 22 source: dbSNP start: 30165002 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165003 feature_type: variation id: rs1601738267 seq_region_name: 22 source: dbSNP start: 30165003 strand: 1 - alleles: - T - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165010 feature_type: variation id: rs772371981 seq_region_name: 22 source: dbSNP start: 30165010 strand: 1 - alleles: - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165011 feature_type: variation id: rs2068246045 seq_region_name: 22 source: dbSNP start: 30165011 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165014 feature_type: variation id: rs1461456166 seq_region_name: 22 source: dbSNP start: 30165014 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165015 feature_type: variation id: rs1371248645 seq_region_name: 22 source: dbSNP start: 30165015 strand: 1 - alleles: - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165020 feature_type: variation id: rs1178402528 seq_region_name: 22 source: dbSNP start: 30165020 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165023 feature_type: variation id: rs953921611 seq_region_name: 22 source: dbSNP start: 30165023 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165025 feature_type: variation id: rs2068246107 seq_region_name: 22 source: dbSNP start: 30165025 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165027 feature_type: variation id: rs2068246130 seq_region_name: 22 source: dbSNP start: 30165027 strand: 1 - alleles: - C - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165028 feature_type: variation id: rs1569344548 seq_region_name: 22 source: dbSNP start: 30165028 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165031 feature_type: variation id: rs2147246080 seq_region_name: 22 source: dbSNP start: 30165031 strand: 1 - alleles: - G - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165034 feature_type: variation id: rs2068246166 seq_region_name: 22 source: dbSNP start: 30165034 strand: 1 - alleles: - G - GG assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165037 feature_type: variation id: rs767640767 seq_region_name: 22 source: dbSNP start: 30165037 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165040 feature_type: variation id: rs2147246083 seq_region_name: 22 source: dbSNP start: 30165040 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165049 feature_type: variation id: rs370676696 seq_region_name: 22 source: dbSNP start: 30165049 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165050 feature_type: variation id: rs1007608945 seq_region_name: 22 source: dbSNP start: 30165050 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165055 feature_type: variation id: rs2068246231 seq_region_name: 22 source: dbSNP start: 30165055 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165057 feature_type: variation id: rs1197464590 seq_region_name: 22 source: dbSNP start: 30165057 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165060 feature_type: variation id: rs2068246262 seq_region_name: 22 source: dbSNP start: 30165060 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165061 feature_type: variation id: rs1484252337 seq_region_name: 22 source: dbSNP start: 30165061 strand: 1 - alleles: - C - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165068 feature_type: variation id: rs1252936167 seq_region_name: 22 source: dbSNP start: 30165068 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165072 feature_type: variation id: rs1195556161 seq_region_name: 22 source: dbSNP start: 30165072 strand: 1 - alleles: - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165078 feature_type: variation id: rs2068246333 seq_region_name: 22 source: dbSNP start: 30165078 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165081 feature_type: variation id: rs1479972144 seq_region_name: 22 source: dbSNP start: 30165081 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165085 feature_type: variation id: rs1258271062 seq_region_name: 22 source: dbSNP start: 30165085 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165086 feature_type: variation id: rs1940229426 seq_region_name: 22 source: dbSNP start: 30165086 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165090 feature_type: variation id: rs1211699949 seq_region_name: 22 source: dbSNP start: 30165090 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165091 feature_type: variation id: rs2068246404 seq_region_name: 22 source: dbSNP start: 30165091 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165096 feature_type: variation id: rs2068246425 seq_region_name: 22 source: dbSNP start: 30165096 strand: 1 - alleles: - CCC - CC assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165098 feature_type: variation id: rs1323551995 seq_region_name: 22 source: dbSNP start: 30165096 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165098 feature_type: variation id: rs1324874125 seq_region_name: 22 source: dbSNP start: 30165098 strand: 1 - alleles: - CTCAATCTCAA - CTCAA assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165108 feature_type: variation id: rs2147246121 seq_region_name: 22 source: dbSNP start: 30165098 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165106 feature_type: variation id: rs1331359257 seq_region_name: 22 source: dbSNP start: 30165106 strand: 1 - alleles: - T - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165111 feature_type: variation id: rs773358585 seq_region_name: 22 source: dbSNP start: 30165111 strand: 1 - alleles: - T - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165116 feature_type: variation id: rs535505556 seq_region_name: 22 source: dbSNP start: 30165116 strand: 1 - alleles: - T - C 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: - G - A 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: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165126 feature_type: variation id: rs2068246592 seq_region_name: 22 source: dbSNP start: 30165126 strand: 1 - alleles: - T - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165127 feature_type: variation id: rs576898868 seq_region_name: 22 source: dbSNP start: 30165127 strand: 1 - alleles: - A - G 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 - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165133 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 - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165141 feature_type: variation id: rs1569344561 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 id: rs972054155 seq_region_name: 22 source: dbSNP start: 30165145 strand: 1 - alleles: - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165149 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 - C 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 seq_region_name: 22 source: dbSNP start: 30165173 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165176 feature_type: variation id: rs1470350617 seq_region_name: 22 source: dbSNP start: 30165176 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165177 feature_type: variation id: rs967170399 seq_region_name: 22 source: dbSNP start: 30165177 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165179 feature_type: variation id: rs1301047588 seq_region_name: 22 source: dbSNP start: 30165179 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165185 feature_type: variation id: rs2147246157 seq_region_name: 22 source: dbSNP start: 30165185 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165190 feature_type: variation id: rs1355551544 seq_region_name: 22 source: dbSNP start: 30165190 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165200 feature_type: variation id: rs1240873024 seq_region_name: 22 source: dbSNP start: 30165200 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165201 feature_type: variation id: rs2068246920 seq_region_name: 22 source: dbSNP start: 30165201 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165203 feature_type: variation id: rs1569344570 seq_region_name: 22 source: dbSNP start: 30165203 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165205 feature_type: variation id: rs1412944780 seq_region_name: 22 source: dbSNP start: 30165205 strand: 1 - alleles: - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165210 feature_type: variation id: rs1181613263 seq_region_name: 22 source: dbSNP start: 30165210 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165212 feature_type: variation id: rs760755875 seq_region_name: 22 source: dbSNP start: 30165212 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165213 feature_type: variation id: rs1285209398 seq_region_name: 22 source: dbSNP start: 30165213 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165214 feature_type: variation id: rs766432868 seq_region_name: 22 source: dbSNP start: 30165214 strand: 1 - alleles: - G - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165215 feature_type: variation id: rs2068247047 seq_region_name: 22 source: dbSNP start: 30165215 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165216 feature_type: variation id: rs911844394 seq_region_name: 22 source: dbSNP start: 30165216 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165217 feature_type: variation id: rs2068247086 seq_region_name: 22 source: dbSNP start: 30165217 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165218 feature_type: variation id: rs944985618 seq_region_name: 22 source: dbSNP start: 30165218 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165219 feature_type: variation id: rs1262010231 seq_region_name: 22 source: dbSNP start: 30165219 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165222 feature_type: variation id: rs2068247136 seq_region_name: 22 source: dbSNP start: 30165222 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165230 feature_type: variation id: rs985071170 seq_region_name: 22 source: dbSNP start: 30165230 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165234 feature_type: variation id: rs1039296342 seq_region_name: 22 source: dbSNP start: 30165234 strand: 1 - alleles: - C - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165235 feature_type: variation id: rs1688321672 seq_region_name: 22 source: dbSNP start: 30165235 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165243 feature_type: variation id: rs922135468 seq_region_name: 22 source: dbSNP start: 30165243 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165244 feature_type: variation id: rs1238072986 seq_region_name: 22 source: dbSNP start: 30165244 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165249 feature_type: variation id: rs2068247250 seq_region_name: 22 source: dbSNP start: 30165249 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165256 feature_type: variation id: rs1198397295 seq_region_name: 22 source: dbSNP start: 30165256 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165257 feature_type: variation id: rs2068247284 seq_region_name: 22 source: dbSNP start: 30165257 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165259 feature_type: variation id: rs1601738352 seq_region_name: 22 source: dbSNP start: 30165259 strand: 1 - alleles: - T - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165273 feature_type: variation id: rs1601738356 seq_region_name: 22 source: dbSNP start: 30165273 strand: 1 - alleles: - T - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165274 feature_type: variation id: rs1333710949 seq_region_name: 22 source: dbSNP start: 30165274 strand: 1 - alleles: - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165275 feature_type: variation id: rs2068247344 seq_region_name: 22 source: dbSNP start: 30165275 strand: 1 - alleles: - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165278 feature_type: variation id: rs2068247358 seq_region_name: 22 source: dbSNP start: 30165278 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165279 feature_type: variation id: rs1393699792 seq_region_name: 22 source: dbSNP start: 30165279 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165284 feature_type: variation id: rs930781754 seq_region_name: 22 source: dbSNP start: 30165284 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165286 feature_type: variation id: rs1401947096 seq_region_name: 22 source: dbSNP start: 30165286 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165288 feature_type: variation id: rs2068247440 seq_region_name: 22 source: dbSNP start: 30165288 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165297 feature_type: variation id: rs2147246196 seq_region_name: 22 source: dbSNP start: 30165297 strand: 1 - alleles: - GG - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165301 feature_type: variation id: rs1453233356 seq_region_name: 22 source: dbSNP start: 30165300 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165308 feature_type: variation id: rs1381904277 seq_region_name: 22 source: dbSNP start: 30165308 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165310 feature_type: variation id: rs1334847323 seq_region_name: 22 source: dbSNP start: 30165310 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165311 feature_type: variation id: rs1049229057 seq_region_name: 22 source: dbSNP start: 30165311 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165312 feature_type: variation id: rs554486539 seq_region_name: 22 source: dbSNP start: 30165312 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165322 feature_type: variation id: rs1158142574 seq_region_name: 22 source: dbSNP start: 30165322 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165325 feature_type: variation id: rs2068247556 seq_region_name: 22 source: dbSNP start: 30165325 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165327 feature_type: variation id: rs1452112275 seq_region_name: 22 source: dbSNP start: 30165327 strand: 1 - alleles: - A - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165330 feature_type: variation id: rs1005000154 seq_region_name: 22 source: dbSNP start: 30165330 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165336 feature_type: variation id: rs1159844263 seq_region_name: 22 source: dbSNP start: 30165336 strand: 1 - alleles: - C - "-" assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165336 feature_type: variation id: rs1370525155 seq_region_name: 22 source: dbSNP start: 30165336 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165338 feature_type: variation id: rs1184558413 seq_region_name: 22 source: dbSNP start: 30165338 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165342 feature_type: variation id: rs374097545 seq_region_name: 22 source: dbSNP start: 30165342 strand: 1 - alleles: - G - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165345 feature_type: variation id: rs116223116 seq_region_name: 22 source: dbSNP start: 30165345 strand: 1 - alleles: - C - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165347 feature_type: variation id: rs906853167 seq_region_name: 22 source: dbSNP start: 30165347 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165348 feature_type: variation id: rs1001496647 seq_region_name: 22 source: dbSNP start: 30165348 strand: 1 - alleles: - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165353 feature_type: variation id: rs903547948 seq_region_name: 22 source: dbSNP start: 30165353 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165354 feature_type: variation id: rs1348313225 seq_region_name: 22 source: dbSNP start: 30165354 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165355 feature_type: variation id: rs145470801 seq_region_name: 22 source: dbSNP start: 30165355 strand: 1 - alleles: - A - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165357 feature_type: variation id: rs1385916721 seq_region_name: 22 source: dbSNP start: 30165357 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165358 feature_type: variation id: rs2147246222 seq_region_name: 22 source: dbSNP start: 30165358 strand: 1 - alleles: - C - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165360 feature_type: variation id: rs1323476935 seq_region_name: 22 source: dbSNP start: 30165360 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165361 feature_type: variation id: rs2068247845 seq_region_name: 22 source: dbSNP start: 30165361 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165362 feature_type: variation id: rs1437372101 seq_region_name: 22 source: dbSNP start: 30165362 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165363 feature_type: variation id: rs2068247886 seq_region_name: 22 source: dbSNP start: 30165363 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165370 feature_type: variation id: rs1327037614 seq_region_name: 22 source: dbSNP start: 30165370 strand: 1 - alleles: - G - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165372 feature_type: variation id: rs957229307 seq_region_name: 22 source: dbSNP start: 30165372 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165379 feature_type: variation id: rs1378914894 seq_region_name: 22 source: dbSNP start: 30165379 strand: 1 - alleles: - T - C assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165380 feature_type: variation id: rs1317945578 seq_region_name: 22 source: dbSNP start: 30165380 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165384 feature_type: variation id: rs2068247974 seq_region_name: 22 source: dbSNP start: 30165384 strand: 1 - alleles: - A - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165397 feature_type: variation id: rs1011379051 seq_region_name: 22 source: dbSNP start: 30165397 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165401 feature_type: variation id: rs1447257451 seq_region_name: 22 source: dbSNP start: 30165401 strand: 1 - alleles: - C - A - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165404 feature_type: variation id: rs557768009 seq_region_name: 22 source: dbSNP start: 30165404 strand: 1 - alleles: - G - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165405 feature_type: variation id: rs1315085643 seq_region_name: 22 source: dbSNP start: 30165405 strand: 1 - alleles: - C - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165410 feature_type: variation id: rs2068248052 seq_region_name: 22 source: dbSNP start: 30165410 strand: 1 - alleles: - A - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165412 feature_type: variation id: rs140139 seq_region_name: 22 source: dbSNP start: 30165412 strand: 1 - alleles: - G - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165416 feature_type: variation id: rs1008056555 seq_region_name: 22 source: dbSNP start: 30165416 strand: 1 - alleles: - C - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165417 feature_type: variation id: rs1476122911 seq_region_name: 22 source: dbSNP start: 30165417 strand: 1 - alleles: - G - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165421 feature_type: variation id: rs1267353088 seq_region_name: 22 source: dbSNP start: 30165421 strand: 1 - alleles: - T - G assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165423 feature_type: variation id: rs1601738416 seq_region_name: 22 source: dbSNP start: 30165423 strand: 1 - alleles: - A - T assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165427 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 - A assembly_name: GRCh37 clinical_significance: [] consequence_type: intron_variant end: 30165435 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 - C 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 - A 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 - C 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 - A 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