{{Rsnum
|rsid=6475
|Chromosome=6
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=CYP21A2
|position=32039426
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CYP21A2
}}{{omim
|id=201910
|rsnum=6475
|variant=0001
}}{{ClinVar
|rsid=6475
|Reversed=0
|FwdREF=T
|FwdALT=A
|REF=T
|ALT=A
|RSPOS=32007203
|CHROM=6
|dbSNPBuildID=52
|SSR=1
|SAO=1
|VP=0x050260000000050102110100
|GENEINFO=CYP21A2:1589
|GENE_NAME=CYP21A2
|GENE_ID=1589
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.32007203T>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;VLD;G5;GNO;OTHERKG;LSD;OM
|CLNACC=RCV000012933.2
|CLNDBN=21-hydroxylase deficiency
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1171; 613815.0001
|Disease=21-hydroxylase deficiency
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1171:C0852654:201910
}}