rs59697075

This variant is located in the CCDC26 gene.

GWAS Catalog Trait Associations (7)

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

lymphocyte percentage of leukocytes

Allele T
OR 0.04
p 3.0e-30
N 171,748
Large GWAS
European

signal-regulatory protein beta-1 measurement

Allele T
OR 0.04
p 7.0e-24
N 47,745
Large GWAS
European

neutrophil gelatinase-associated lipocalin measurement

Allele T
OR 0.05
p 2.0e-19
N 47,745
Large GWAS
European

peptidoglycan recognition protein 1 measurement

Allele T
OR 0.04
p 5.0e-16
N 47,745
Large GWAS
European

leukocyte quantity

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele C
OR 0.03
p 2.0e-61
N 504,825
Large GWAS
multi-ancestry
Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele C
OR 0.03
p 2.0e-30
N 408,112
Large GWAS
European
Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele C
OR 0.05
p 3.0e-62
N 381,267
Major Consortium StudyLarge GWAS
European

myeloid leukocyte count

Allele T
OR 0.04
p 2.0e-85
N 562,243
Large GWAS
European
Allele T
OR 0.05
p 5.0e-39
N 169,219
Large GWAS
European

neutrophil count

Allele T
OR 0.04
p 6.0e-80
N 519,288
Large GWAS
European
Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele T
OR 0.04
p 2.0e-57
N 408,112
Large GWAS
European
Allele T
OR 0.03
p 2.0e-55
N 394,642
Large GWAS
European
Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele T
OR 0.04
p 3.0e-42
N 275,068
Major Consortium StudyLarge 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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