rs4609139
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. “Meta-analysis of genome-wide scans for total body BMD in children and adults reveals allelic heterogeneity and age-specific effects at the WNT16 locus.” Plos Genetics 8(7):e1002718 (2012)
Allele T
OR —
β 0.081
p 1.0e-10
N 2,659
Meta-analysis
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…