{{Rsnum
|rsid=151344503
|Chromosome=6
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CYP21A2
|position=32040766
|Gene_s=CYP21A2,TNXB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=6
|CLNACC=RCV000012953.1
|CLNALLE=1
|CLNDBN=21-hydroxylase deficiency
|CLNHGVS=NC_000006.11:g.32008543G>A
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=613815.0022
|Disease=21-hydroxylase deficiency
|FwdALT=A
|FwdREF=G
|GENEINFO=TNXB:7148; CYP21A2:1589
|GENE_ID=7148; 1589
|GENE_NAME=TNXB; CYP21A2
|REF=G
|RSPOS=32008543
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD
|VC=SNV
|VP=0x050260000000000002100100
|WGT=0
|dbSNPBuildID=133
|rsid=151344503
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1171:C0852654:201910
}}