rs104894069
A SNP in the CYP11B1 gene on chromosome 8. Its most notable genotype is G;G: common in clinvar
- Gene
- CYP11B1
- Location
- Chr 8142,879,690 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs104894069 on the minus strand: (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Notes
From SNPedia
Notes
[The water supply of SPF animal houses. I. Methods for the hygienic improvement of drinking water. II. Suitability of various filtration systems for water sterilization]. CYP11B1 mutations causing non-classic adrenal hyperplasia due to 11 beta-hydroxylase deficiency. Hormonal hypertension in children: 11beta-hydroxylase deficiency and apparent mineralocorticoid excess. Steroid 11 beta-hydroxylase deficiency and related disorders. Donor splice mutation in the 11beta-hydroxylase (CypllB1) gene resulting in sex reversal: a case report and review of the literature. A bioinformatics approach for the phenotype prediction of nonsynonymous single nucleotide polymorphisms in human cytochromes P450.
Source and license
Adapted from rs104894069 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.