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