rs884373
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.
facial morphology trait
White JD et al. “Insights into the genetic architecture of the human face.” Nature Genetics 53(1):45-53 (2021)
Allele T
OR —
p 7.0e-17
N 4,680
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.
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