rs3802230
This is a intron variant variant in the CYP11B2 gene.
▶GWAS Catalog Trait Associations (6)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (6)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
diastolic blood pressure
systolic blood pressure
androstenedione measurement
body height
mean arterial pressure
pulse pressure measurement
▶ClinVar annotation
Corticosterone 18-monooxygenase deficiency; Corticosterone methyloxidase type 2 deficiency; Glucocorticoid-remediable aldosteronism
View on ClinVar →About CYP11B2
This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the mitochondrial inner membrane. The enzyme has steroid 18-hydroxylase activity to synthesize aldosterone and 18-oxocortisol as well as steroid 11 beta-hydroxylase activity. Mutations in this gene cause corticosterone methyl oxidase deficiency. [provided by RefSeq, Jul 2008]
View all CYP11B2 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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