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