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