[{"ambiguity":"R","ancestral_allele":"G","MAF":0.294928,"minor_allele":"A","name":"rs699","clinical_significance":["benign","risk factor"],"most_severe_consequence":"missense_variant","mappings":[{"end":230845794,"coord_system":"chromosome","allele_string":"A/G","location":"1:230845794-230845794","assembly_name":"GRCh37","start":230845794,"seq_region_name":"1","strand":1}],"source":"Variants (including SNPs and indels) imported from dbSNP","synonyms":["VAR_007096","NP_000020.1:p.Met268Thr","NM_000029.3:c.803T>C","106150.0001","rs3182295","rs386606420","rs61617185","rs4714","rs17856353","PA166153539","RCV000405686","RCV000019693","RCV000242838","RCV000019692","RCV000019691"],"var_class":"SNP","evidence":["Frequency","HapMap","1000Genomes","Cited","ESP","Phenotype_or_Disease","ExAC","TOPMed","gnomAD"]}]