{{Rsnum
|rsid=397509367
|Chromosome=6
|position=32041097
|Orientation=plus
|geno1=(C;C)
|geno2=(C;GG)
|geno3=(GG;GG)
|Gene=CYP21A2
|Gene_s=CYP21A2,TNXB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=CC
|CHROM=6
|CLNACC=RCV000012941.1
|CLNALLE=1
|CLNDBN=21-hydroxylase deficiency
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1171:C0852654:201910
|CLNHGVS=NC_000006.11:g.32008874_32008875delGGinsC
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=613815.0008
|Disease=21-hydroxylase deficiency
|FwdALT=C
|FwdREF=GG
|REF=CGG
|RSPOS=32008873
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD
|VC=DIV
|VP=0x050060000000000002100200
|WGT=0
|dbSNPBuildID=136
|rsid=397509367
|GENEINFO=TNXB:7148; CYP21A2:1589
|GENE_ID=7148; 1589
|GENE_NAME=TNXB; CYP21A2
}}