{"mappings":[{"strand":1,"ancestral_allele":"C","start":133256042,"coord_system":"chromosome","assembly_name":"GRCh38","allele_string":"C/T","location":"9:133256042-133256042","end":133256042,"seq_region_name":"9"},{"coord_system":"chromosome","start":133256189,"assembly_name":"GRCh38","strand":1,"ancestral_allele":null,"location":"CHR_HG2030_PATCH:133256189-133256189","end":133256189,"seq_region_name":"CHR_HG2030_PATCH","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,"var_class":"SNP","name":"rs56116432","evidence":["Frequency","1000Genomes","ESP","ExAC","TOPMed","gnomAD"],"minor_allele":"T","most_severe_consequence":"missense_variant","source":"Variants (including SNPs and indels) imported from dbSNP","ambiguity":"Y"}