rs57683624
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.
eosinophil count
Höglund J et al. “Gene-Based Variant Analysis of Whole-Exome Sequencing in Relation to Eosinophil Count.” Frontiers in Immunology 13:862255 (2022)
Allele A
OR 0.04
p 8.0e-10
N 365,954
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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