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