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