rs505429

This is a intron variant variant in the TMEM135 gene.

GWAS Catalog Trait Associations (6)

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

bone tissue density

Allele G
OR 0.10
p 2.0e-29
N 31,873
Large GWAS
European

sclerostin measurement

Allele G
OR 0.04
p 1.0e-12
N 47,745
Large GWAS
European

spine bone mineral density

Allele G
OR 0.06
p 5.0e-11
N 31,986
Large GWAS
European

trunk bone mineral density

Allele G
OR 0.06
p 5.0e-11
N 31,986
Large GWAS
European

pelvis bone mineral density

Allele G
OR 0.05
p 4.0e-9
N 31,873
Large GWAS
European

alkaline phosphatase measurement

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele G
OR 0.01
p 2.0e-8
N 463,178
Large GWAS
multi-ancestry

About TMEM135

Predicted to enable lipid transporter activity. Predicted to be involved in several processes, including fatty acid derivative transport; fatty acid metabolic process; and long-chain fatty acid transport. Predicted to act upstream of or within several processes, including regulation of oxidative phosphorylation; response to food; and retinal pigment epithelium development. Predicted to be located in peroxisome. Predicted to be active in peroxisomal membrane. [provided by Alliance of Genome Resources, Apr 2025]

View all TMEM135 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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