rs8005161

This is a regulatory region variant variant in the GPR65 gene.

GWAS Catalog Trait Associations (3)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

Crohn's disease

Allele T
OR 1.23
p 4.0e-18
N 21,389
Meta-analysisLarge GWAS
European
Allele T
OR 1.17
p 9.0e-14
N 20,883
Large GWAS
multi-ancestry

inflammatory bowel disease

Allele T
OR 1.15
p 2.0e-14
N 34,366
Large GWAS
European

About GPR65

Enables G protein-coupled receptor activity. Involved in several processes, including activation of GTPase activity; positive regulation of stress fiber assembly; and response to acidic pH. Located in plasma membrane. [provided by Alliance of Genome Resources, Apr 2025]

View all GPR65 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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