rs56335989
This is a intron variant variant in the CPED1 gene.
▶GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
bone tissue density
Medina-Gomez C et al. “Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis.” Communications Biology 6(1):691 (2023)
Allele T
OR —
β 0.051
p 2.0e-8
N 43,832
Large GWAS
European
About CPED1
Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Jul 2025]
View all CPED1 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…