rs61784824

This is a intron variant variant in the IPP 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 0.09
p 2.0e-8
N 9,675
Meta-analysis
multi-ancestry

About IPP

The protein encoded by this gene is a member of the kelch family of proteins, which is characterized by a 50 amino acid repeat which interacts with actin. Transcript variants have been described but their full-length nature has not been determined. [provided by RefSeq, Jul 2008]

View all IPP variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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