rs7240554

This is a intron variant variant in the NOL4 gene.

GWAS Catalog Trait Associations (1)

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

insomnia

Allele T
OR 0.01
p 1.0e-8
N 1,216,033
Meta-analysisLarge GWAS
European

About NOL4

Predicted to enable RNA binding activity. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Jul 2025]

View all NOL4 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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