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