rs117733138

This is a intron variant variant in the BTBD9 gene.

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GWAS Catalog Trait Associations (1)

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

sleep apnea measurement

Xu H et al. “Genome-Wide Association Study of Obstructive Sleep Apnea and Objective Sleep-related Traits Identifies Novel Risk Loci in Han Chinese Individuals.” American Journal of Respiratory and Critical Care Medicine 206(12):1534-1545 (2022)

Allele G

OR 0.40

p 5.0e-9

N 6,246

Large GWAS

East Asian

About BTBD9

This locus encodes a BTB/POZ domain-containing protein. This domain is known to be involved in protein-protein interactions. Polymorphisms at this locus have been reported to be associated with susceptibility to Restless Legs Syndrome and may also be associated with Tourette Syndrome. Alternatively spliced transcript variants have been described. [provided by RefSeq, Aug 2011]

View all BTBD9 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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