rs3117581

This is a downstream gene variant variant in the APOM gene.

GWAS Catalog Trait Associations (2)

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

forced expiratory volume, 25-hydroxyvitamin D3 measurement

Allele G
OR
p 9.0e-18
N 115,312
Meta-analysisLarge GWAS
multi-ancestry

Inguinal hernia

Allele A
OR 1.11
p 3.0e-10
N 275,546
Major Consortium StudyLarge GWAS
European

About APOM

The protein encoded by this gene is an apolipoprotein and member of the lipocalin protein family. It is found associated with high density lipoproteins and to a lesser extent with low density lipoproteins and triglyceride-rich lipoproteins. The encoded protein is secreted through the plasma membrane but remains membrane-bound, where it is involved in lipid transport. Alternate splicing results in both coding and non-coding variants of this gene. [provided by RefSeq, Jan 2012]

View all APOM variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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