rs144818546

This is a intron variant variant in the PHLPP2 gene.

GWAS Catalog Trait Associations (1)

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

interleukin-34 measurement

Allele G
OR 0.32
p 4.0e-13
N 47,745
Large GWAS
European

About PHLPP2

Predicted to enable metal ion binding activity and phosphoprotein phosphatase activity. Predicted to be involved in intracellular signal transduction. Located in several cellular components, including cilium; intercellular bridge; and mitotic spindle. [provided by Alliance of Genome Resources, Apr 2025]

View all PHLPP2 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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