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