rs79782206
This is a regulatory region variant variant in the CCDC33 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.
color vision disorder
Nardone GG et al. “Identifying missing pieces in color vision defects: a genome-wide association study in Silk Road populations.” Frontiers in Genetics 14:1161696 (2023)
Allele T
OR 0.25
p 1.0e-8
N 520
Small GWAS
Other
About CCDC33
Predicted to be active in peroxisome. [provided by Alliance of Genome Resources, Jul 2025]
View all CCDC33 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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