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