rs13415724

This is a intron variant variant in the THSD7B 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-11
N 2,365,010
Meta-analysisLarge GWAS
European

About THSD7B

Predicted to be involved in actin cytoskeleton organization. Predicted to be located in membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]

View all THSD7B variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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