{{Rsnum
|rsid=193922539
|Chromosome=8
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CYP11B1
|position=142879163
|Gene_s=CYP11B1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922539
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=143960579
|CHROM=8
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050268000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.143960579C>T
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Congenital adrenal hyperplasia
|Disease=Congenital adrenal hyperplasia
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000029645.1
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0001627:237751000
|GENEINFO=CYP11B1:1584
|GENE_ID=1584
|GENE_NAME=CYP11B1
}}{{PMID Auto
|PMID=20089618
|Title=Functional consequences of seven novel mutations in the CYP11B1 gene: four mutations associated with nonclassic and three mutations causing classic 11{beta}-hydroxylase deficiency.
|OA=1
}}