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.

diastolic blood pressure

Allele A
OR 0.15
p 3.0e-24
N 1,028,980
Large GWAS
multi-ancestry
Allele A
OR 0.02
p 4.0e-19
N 1,212,859
Large GWAS
European

systolic blood pressure

Allele A
OR 0.24
p 8.0e-24
N 1,028,980
Large GWAS
multi-ancestry

body height

Allele C
OR 0.01
p 1.0e-15
N 405,540
Large GWAS
European

mean arterial pressure

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele A
OR 0.01
p 1.0e-14
N 506,365
Large GWAS
multi-ancestry

pulse pressure measurement

Allele A
OR 0.10
p 1.0e-8
N 1,028,980
Large GWAS
multi-ancestry

ClinVar annotation

Benign☆☆☆
2 submitters1 publication

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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