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