rs75125057

This is a intron variant variant in the TTC39A gene.

GWAS Catalog Trait Associations (1)

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

About TTC39A

Located in centrosome. [provided by Alliance of Genome Resources, Jul 2025]

View all TTC39A variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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