rs143001709

This is a intron variant variant in the C15orf39 gene.

GWAS Catalog Trait Associations (1)

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

About C15orf39

Located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]

View all C15orf39 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

Sign in to join the discussion.

Loading comments…