rs17591211

This is a intron variant variant in the MAIP1 gene.

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GWAS Catalog Trait Associations (1)

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

hip geometry

Faber BG et al. “The genetic architecture of hip shape and its role in the development of hip osteoarthritis and fracture.” Human Molecular Genetics 34(3):207-217 (2025)

Allele A

OR 0.04

p 3.0e-9

N 43,485

Large GWAS

multi-ancestry

About MAIP1

Predicted to enable ribosome binding activity. Involved in calcium import into the mitochondrion; mitochondrial calcium ion homeostasis; and protein insertion into mitochondrial membrane. Located in mitochondrial matrix. [provided by Alliance of Genome Resources, Jul 2025]

View all MAIP1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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