rs186407219

This is a intron variant variant in the PITPNM2 gene.

GWAS Catalog Trait Associations (1)

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

appendicular lean mass

Allele A
OR 0.13
p 1.0e-9
N 450,243
Major Consortium StudyLarge GWAS
European

About PITPNM2

PITPNM2 belongs to a family of membrane-associated phosphatidylinositol transfer domain-containing proteins that share homology with the Drosophila retinal degeneration B (rdgB) protein (Ocaka et al., 2005 [PubMed 15627748]).[supplied by OMIM, Mar 2008]

View all PITPNM2 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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