{{Rsnum
|rsid=6471
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Chromosome=6
|Orientation=plus
|Gene=CYP21A2
|position=32040110
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CYP21A2
}}{{PMID Auto
|PMID=20617557
|Title=Functional polymorphisms in the CYP3A4, CYP3A5, and CYP21A2 genes in the risk for hypertension in pregnancy
}}
{{PMID Auto
|PMID=20685352
|Title=Functional polymorphisms in the CYP3A4, CYP3A5, and CYP21A2 genes in the risk for hypertension in pregnancy
}}
{{omim
|id=201910
|rsnum=6471
|variant=0002
}}{{ClinVar
|rsid=6471
|Reversed=0
|FwdREF=G
|FwdALT=C,T
|REF=G
|ALT=C,T
|RSPOS=32007887
|CHROM=6
|dbSNPBuildID=52
|SSR=1
|SAO=1
|VP=0x050268000000030102110100
|GENEINFO=CYP21A2:1589
|GENE_NAME=CYP21A2
|GENE_ID=1589
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000006.11:g.32007887G>C; NC_000006.11:g.32007887G>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;PMC;S3D;G5A;G5;GNO;OTHERKG;LSD;OM
|CLNACC=RCV000055820.1; RCV000012934.2; RCV000012935.1; RCV000012936.1
|CLNDBN=21-hydroxylase deficiency; Adenoma, cortisol-producing; Carcinoma, adrenocortical, androgen-secreting
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1171:C0852654:201910
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1171; 613815.0002
|Disease=21-hydroxylase deficiency; Adenoma; Carcinoma
}}{{GET Evidence
|gene=NM_000500
|aa_change=Leu278Val
|aa_change_short=L278V
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs6471
|n_genomes=1
|n_genomes_annotated=0
|n_haplomes=1
|n_articles=0
|n_articles_annotated=0
|nblosum100=0
|autoscore=1
|webscore=N
}}