{"source":"Variants (including SNPs and indels) imported from dbSNP","evidence":["Frequency","1000Genomes","Cited","ESP","ExAC","TOPMed","gnomAD"],"minor_allele":null,"var_class":"SNP","ambiguity":"Y","synonyms":["rs57404253","VAR_022246","PA166282682"],"most_severe_consequence":"missense_variant","name":"rs8065080","mappings":[{"coord_system":"chromosome","end":3577153,"location":"17:3577153-3577153","assembly_name":"GRCh38","ancestral_allele":"C","strand":1,"allele_string":"T/C","start":3577153,"seq_region_name":"17"}],"MAF":null}