rs2413887
This is a upstream gene variant variant in the CTXN2 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.
benign neoplasm of eye
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 0.52
p 4.0e-21
N 58,987
Major Consortium StudyLarge GWAS
Hispanic or Latin American
skin cancer
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 0.31
p 2.0e-12
N 58,901
Major Consortium StudyLarge GWAS
Hispanic or Latin American
Dermatochalasis
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 0.26
p 3.0e-11
N 625,298
Major Consortium StudyLarge GWAS
multi-ancestry
About CTXN2
Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
View all CTXN2 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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