rs4911242
This is a regulatory region variant variant in the NOL4L 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.
cup-to-disc ratio measurement
Alipanahi B et al. “Large-scale machine-learning-based phenotyping significantly improves genomic discovery for optic nerve head morphology.” American Journal of Human Genetics 108(7):1217-1230 (2021)
Allele A
OR 0.00
p 4.0e-9
N 65,680
Large GWAS
European
About NOL4L
Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
View all NOL4L variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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