{{Rsnum
|rsid=6445
|Chromosome=6
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CYP21A2
|position=32041006
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CYP21A2,TNXB
}}{{omim
|id=201910
|rsnum=6445
|variant=0010
}}{{ClinVar
|rsid=6445
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=32008783
|CHROM=6
|dbSNPBuildID=52
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=TNXB:7148; CYP21A2:1589
|GENE_NAME=TNXB; CYP21A2
|GENE_ID=7148; 1589
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.32008783C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000012943.2
|CLNDBN=21-hydroxylase deficiency
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1171; 613815.0010
|Disease=21-hydroxylase deficiency
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1171:C0852654:201910
}}

{{on chip | 23andMe v4}}