{{Rsnum
|rsid=111647200
|Chromosome=6
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=CYP21A2
|position=32039807
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CYP21A2
}}{{ClinVar
|ALT=A
|CHROM=6
|CLNACC=RCV000012947.1
|CLNALLE=1
|CLNDBN=21-hydroxylase deficiency
|CLNHGVS=NC_000006.11:g.32007584T>A
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=613815.0016
|Disease=21-hydroxylase deficiency
|FwdALT=A
|FwdREF=T
|GENEINFO=CYP21A2:1589
|GENE_ID=1589
|GENE_NAME=CYP21A2
|REF=T
|RSPOS=32007584
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;S3D;GNO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000102110100
|WGT=0
|dbSNPBuildID=132
|rsid=111647200
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1171:C0852654:201910
}}