{{Rsnum
|rsid=267606757
|Chromosome=6
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=CYP21A2
|position=32039162
|Gene_s=CYP21A2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=6
|CLNACC=RCV000012966.1
|CLNALLE=1
|CLNDBN=21-hydroxylase deficiency
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1171:C0852654:201910
|CLNHGVS=NC_000006.11:g.32006939A>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=613815.0035
|Disease=21-hydroxylase deficiency
|FwdALT=C
|FwdREF=A
|GENEINFO=CYP21A2:1589
|GENE_ID=1589
|GENE_NAME=CYP21A2
|REF=A
|RSPOS=32006939
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606757
}}