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