rs9830553

This is a intron variant variant in the CCDC13 gene.

GWAS Catalog Trait Associations (1)

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

atrial fibrillation

Allele A
OR 0.02
p 8.0e-9
N 1,840,341
Large GWAS
European

About CCDC13

Acts upstream of or within DNA damage response; cytoplasmic microtubule organization; and non-motile cilium assembly. Located in centriolar satellite. [provided by Alliance of Genome Resources, Jul 2025]

View all CCDC13 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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