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