{"synonyms":[],"minor_allele":null,"source":"Variants (including SNPs and indels) imported from dbSNP","name":"rs116035550","MAF":null,"evidence":["Frequency","1000Genomes","ESP","ExAC","TOPMed","gnomAD"],"ambiguity":"V","most_severe_consequence":"missense_variant","var_class":"SNP","population_genotypes":[{"population":"ESP6500:EA","frequency":0.0002326,"genotype":"A|G","count":1},{"frequency":0.9998,"population":"ESP6500:EA","genotype":"G|G","count":4299},{"frequency":1,"population":"ESP6500:AA","genotype":"G|G","count":2202}],"mappings":[{"seq_region_name":"11","coord_system":"chromosome","assembly_name":"GRCh37","strand":1,"end":212464,"ancestral_allele":"G","location":"11:212464-212464","start":212464,"allele_string":"G/A/C"}]}