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