{"name":"rs56116432","source":"Variants (including SNPs and indels) imported from dbSNP","minor_allele":"T","evidence":["Frequency","1000Genomes","Cited","ESP","ExAC","TOPMed","gnomAD"],"ambiguity":"H","var_class":"SNP","most_severe_consequence":"missense_variant","mappings":[{"location":"9:133256042-133256042","assembly_name":"GRCh38","ancestral_allele":"C","coord_system":"chromosome","seq_region_name":"9","end":133256042,"start":133256042,"allele_string":"C/A/T","strand":1},{"allele_string":"C/A/T","strand":1,"start":82135,"end":82135,"location":"HG2030_PATCH:82135-82135","assembly_name":"GRCh38","ancestral_allele":null,"seq_region_name":"HG2030_PATCH","coord_system":"scaffold"}],"MAF":0.00274725,"synonyms":[]}