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