rs10956483
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
Okada Y et al. “Identification of nine novel loci associated with white blood cell subtypes in a Japanese population.” Plos Genetics 7(6):e1002067 (2011)
Allele C
OR 0.07
p 2.0e-10
N 8,794
Large GWAS
East Asian
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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