{"var_class":"SNP","minor_allele":"G","ambiguity":"S","synonyms":["rs74298253","NM_001278635.1:c.1281G>A","NM_001278634.2:c.1203G>A","NM_001278633.1:c.1281G>A","NM_001278632.1:c.1203G>A","NM_016358.2:c.1203G>A","NM_016358.3:c.1203G>A","NM_001278634.1:c.1203G>A","NM_001278635.2:c.1281G>A"],"mappings":[{"allele_string":"C/G","seq_region_name":"6","assembly_name":"GRCh38","ancestral_allele":"C","location":"6:104936103-104936103","start":104936103,"end":104936103,"coord_system":"chromosome","strand":1}],"most_severe_consequence":"intron_variant","MAF":0.310832,"evidence":["Frequency","1000Genomes","Cited","Phenotype_or_Disease","TOPMed","gnomAD"],"name":"rs2095812","source":"Variants (including SNPs and indels) imported from dbSNP"}