rs11998606

This variant is located in the PINX1 gene.

GWAS Catalog Trait Associations (14)

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

triglyceride measurement

Allele C
OR 0.04
p 3.0e-17
N 115,082
Large GWAS
European

fatty acid amount

Allele C
OR 0.02
p 2.0e-9
N 115,006
Large GWAS
European

blood VLDL cholesterol amount

Allele C
OR 0.02
p 6.0e-9
N 115,082
Large GWAS
European

About PINX1

Enables telomerase RNA binding activity and telomerase inhibitor activity. Involved in several processes, including negative regulation of macromolecule metabolic process; positive regulation of protein localization to nucleolus; and protein localization to organelle. Acts upstream of or within telomere maintenance via telomerase. Located in several cellular components, including chromosomal region; nuclear lumen; and spindle. Implicated in hepatocellular carcinoma. [provided by Alliance of Genome Resources, Apr 2025]

View all PINX1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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