rs34537746

This variant is located in the R3HDM2 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 1,409,137
Meta-analysisLarge GWAS
European

About R3HDM2

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

View all R3HDM2 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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