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