[{"source":"Variants (including SNPs and indels) imported from dbSNP","minor_allele":"A","evidence":["Frequency","1000Genomes","Cited","ESP","Phenotype_or_Disease","ExAC","TOPMed","gnomAD"],"mappings":[{"ancestral_allele":"G","end":230710048,"seq_region_name":"1","assembly_name":"GRCh38","coord_system":"chromosome","allele_string":"A/G","start":230710048,"location":"1:230710048-230710048","strand":1}],"var_class":"SNP","ambiguity":"R","clinical_significance":["benign","risk factor"],"MAF":0.2949,"most_severe_consequence":"missense_variant","synonyms":["106150.0001","rs3182295","rs61617185","rs17856353","rs386606420","rs4714","VCV000018068","RCV000405686","RCV000019693","RCV000019692","RCV000019691","RCV000242838","RCV000835695","VAR_007096","PA166153539","NM_000029.4:c.803T>C","NP_000020.1:p.Met268Thr","NM_000029.3:c.803T>C"],"name":"rs699"}]