rs9369062

This is a intron variant variant in the BTBD9 gene.

▶

GWAS Catalog Trait Associations (1)

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

physical activity measurement

Qi G et al. “Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms.” Genetic Epidemiology 46(2):122-138 (2022)

Allele C

OR —

β 0.037

p 2.0e-12

N 88,411

Large GWAS

European

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.

Community Wiki

No community notes yet for this variant. Sign in to start one.

Comments

Loading comments…