rs17328181

This is a intron variant variant in the FUNDC2 gene.

GWAS Catalog Trait Associations (1)

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

venous thromboembolism

Allele G
OR 0.07
p 3.0e-9
N 1,063,277
Meta-analysisLarge GWAS
multi-ancestry

About FUNDC2

Enables phosphatidylinositol-3,4,5-trisphosphate binding activity. Involved in intracellular triglyceride homeostasis. Located in mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]

View all FUNDC2 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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