rs141403654

This is a intron variant variant in the AGBL2 gene.

GWAS Catalog Trait Associations (1)

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

age-related hearing impairment

Allele A
OR 0.02
p 3.0e-8
N 723,266
Meta-analysisLarge GWAS
European

About AGBL2

Predicted to enable metallocarboxypeptidase activity and tubulin binding activity. Predicted to be involved in protein side chain deglutamylation. Located in centriole and ciliary basal body. [provided by Alliance of Genome Resources, Jul 2025]

View all AGBL2 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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