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