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