{{Rsnum
|rsid=6467
|Gene=CYP21A2
|Chromosome=6
|position=32039081
|Orientation=minus
|GMAF=0.3356
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=CYP21A2
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 0.0 | 0.0 | 0.0
| HCB | 10.7 | 43.5 | 45.8
| JPT | 13.0 | 42.6 | 44.4
| YRI | 4.9 | 44.4 | 50.7
| ASW | 0.0 | 0.0 | 0.0
| CHB | 10.7 | 43.5 | 45.8
| CHD | 10.6 | 50.0 | 39.4
| GIH | 0.0 | 0.0 | 0.0
| LWK | 13.0 | 50.0 | 37.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}
{{PMID Auto
|PMID=19654554
|Title=The Major Histocompatibility Complex Conserved Extended Haplotype 8.1 in AIDS-Related Non-Hodgkin Lymphoma
|OA=1
}}

{{ClinVar
|ALT=A,G
|CAF=0.3356; 0.6644; .
|CHROM=6
|CLNACC=RCV000012939.2
|CLNALLE=2
|CLNDBN=21-hydroxylase deficiency
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1171:C0852654:201910
|CLNHGVS=NC_000006.11:g.32006858C>G
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1171; 613815.0006
|COMMON=1
|Disease=21-hydroxylase deficiency
|FwdALT=C,T
|FwdREF=G
|GENEINFO=CYP21A2:1589
|GENE_ID=1589
|GENE_NAME=CYP21A2
|REF=C
|RSPOS=32006858
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;SLO;VLD;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD;OM
|VC=SNV
|VP=0x05016800000015051f110100
|WGT=0
|dbSNPBuildID=52
|rsid=6467
}}

{{PMID Auto
|PMID=25249698
|Title=CYP21A2 polymorphisms in patients with autoimmune Addison's disease, and linkage disequilibrium to HLA risk alleles
}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}