{{Rsnum
|rsid=9378251
|Chromosome=6
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=C4B
|position=32038514
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CYP21A2
}}{{omim
|id=201910
|rsnum=9378251
|variant=0004
}}{{ClinVar
|rsid=9378251
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=32006291
|CHROM=6
|dbSNPBuildID=119
|SSR=0
|SAO=1
|VP=0x050260000000070102110100
|GENEINFO=CYP21A2:1589
|GENE_NAME=CYP21A2
|GENE_ID=1589
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.32006291C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;VLD;G5A;G5;GNO;OTHERKG;LSD;OM
|CLNACC=RCV000012938.3
|CLNDBN=21-hydroxylase deficiency
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1171:C0852654:201910
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1171; 613815.0004
|Disease=21-hydroxylase deficiency
}}