rs13067055

This is a intron variant variant in the MOBP gene.

GWAS Catalog Trait Associations (2)

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

appendicular lean mass

Allele A
OR 0.01
p 2.0e-11
N 450,243
Major Consortium StudyLarge GWAS
European

neuroimaging measurement

Allele G
OR 0.06
p 4.0e-9
N 21,282
Major Consortium StudyLarge GWAS
European

About MOBP

Predicted to be a structural constituent of myelin sheath. Predicted to be involved in nervous system development. Predicted to be located in mitochondrion and perinuclear region of cytoplasm. Implicated in frontotemporal dementia. [provided by Alliance of Genome Resources, Jul 2025]

View all MOBP variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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