rs77521439
This is a intron variant variant in the CCDC26 gene.
▶GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
monocyte count
Loya H et al. “A scalable variational inference approach for increased mixed-model association power.” Nature Genetics 57(2):461-468 (2025)
Allele A
OR 0.11
p 2.0e-13
N 394,642
Large GWAS
European
About CCDC26
Implicated in brain cancer and high grade glioma. [provided by Alliance of Genome Resources, Jul 2025]
View all CCDC26 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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