rs10479170

This is a intron variant variant in the FAM13B gene.

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GWAS Catalog Trait Associations (1)

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

balding measurement

Yap CX et al. “Dissection of genetic variation and evidence for pleiotropy in male pattern baldness.” Nature Communications 9(1):5407 (2018)

Allele G

OR 0.02

p 7.0e-9

N 205,327

Large GWAS

European

About FAM13B

Predicted to enable GTPase activator activity. Predicted to be involved in regulation of small GTPase mediated signal transduction. Predicted to be located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]

View all FAM13B variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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