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