rs2265211

This is a intron variant variant in the EEF1AKMT1 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 2.0e-10
N 2,365,010
Meta-analysisLarge GWAS
European

About EEF1AKMT1

Enables protein-lysine N-methyltransferase activity. Involved in peptidyl-lysine methylation. Predicted to be located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]

View all EEF1AKMT1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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