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