{{Rsnum
|rsid=12530380
|Chromosome=6
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=CYP21A2
|position=32039810
|Gene_s=CYP21A2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 0.0 | 0.0 | 100.0
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{ClinVar
|rsid=12530380
|Reversed=0
|FwdREF=T
|FwdALT=A
|REF=T
|ALT=A
|RSPOS=32007587
|CHROM=6
|dbSNPBuildID=120
|SSR=0
|SAO=1
|VP=0x050260000000070503110100
|GENEINFO=CYP21A2:1589
|GENE_NAME=CYP21A2
|GENE_ID=1589
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.32007587T>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;VLD;G5A;G5;HD;GNO;OTHERKG;PH3;LSD;OM
|CLNACC=RCV000012947.1; RCV000055823.1
|CLNDBN=21-hydroxylase deficiency
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1171; 613815.0016
|Disease=21-hydroxylase deficiency
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1171:C0852654:201910
}}

{{omim
|id=201910
|rsnum=12530380
|variant=0017
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}