[{"clinical_significance":["benign","risk factor"],"synonyms":["106150.0001","VAR_007096","rs386606420","rs4714","rs3182295","rs17856353","rs61617185","PA166153539","RCV000835695","RCV000019692","RCV000405686","RCV002259306","RCV000242838","RCV000019691","RCV000019693","VCV000018068","NM_001384479.1:c.776T>C","NP_001371408.1:p.Met259Thr","NM_001382817.3:c.776T>C","NM_000029.3:c.803T>C","NP_001369746.2:p.Met259Thr","NM_001382817.1:c.803T>C","NM_000029.4:c.803T>C","NM_001382817.2:c.776T>C"],"MAF":0.294928,"mappings":[{"ancestral_allele":"G","coord_system":"chromosome","start":230845794,"assembly_name":"GRCh37","strand":1,"allele_string":"A/G","seq_region_name":"1","location":"1:230845794-230845794","end":230845794}],"most_severe_consequence":"missense_variant","name":"rs699","var_class":"SNP","source":"Variants (including SNPs and indels) imported from dbSNP","evidence":["Frequency","1000Genomes","Cited","ESP","Phenotype_or_Disease","ExAC","TOPMed","gnomAD"],"minor_allele":"A","ambiguity":"R"}]