{"source":"Variants (including SNPs and indels) imported from dbSNP","evidence":["Frequency","1000Genomes","ESP","ExAC","TOPMed","gnomAD"],"minor_allele":"T","mappings":[{"assembly_name":"GRCh38","end":133256042,"seq_region_name":"9","ancestral_allele":"C","strand":1,"location":"9:133256042-133256042","start":133256042,"allele_string":"C/T","coord_system":"chromosome"},{"coord_system":"chromosome","allele_string":"C/T","start":133256189,"location":"CHR_HG2030_PATCH:133256189-133256189","strand":1,"ancestral_allele":null,"seq_region_name":"CHR_HG2030_PATCH","end":133256189,"assembly_name":"GRCh38"}],"MAF":0.002596,"most_severe_consequence":"missense_variant","var_class":"SNP","ambiguity":"Y","name":"rs56116432","synonyms":["NP_065202.2:p.Gly230Asp","NM_020469.3:c.689G>A","NM_020469.2:c.689G>A"]}