rs138628047
This is a intron variant variant in the CCDC26 gene.
▶GWAS Catalog Trait Associations (3)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (3)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
monocyte percentage of leukocytes
Astle WJ et al. “The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.” Cell 167(5):1415-1429.e19 (2016)
Allele C
OR 0.18
p 2.0e-16
N 170,494
Large GWAS
European
granulocyte percentage of myeloid white cells
Astle WJ et al. “The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.” Cell 167(5):1415-1429.e19 (2016)
Allele C
OR 0.17
p 6.0e-16
N 169,545
Large GWAS
European
monocyte count
Astle WJ et al. “The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.” Cell 167(5):1415-1429.e19 (2016)
Allele C
OR 0.15
p 2.0e-11
N 170,721
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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