rs798943
This is a intron variant variant in the CPED1 gene.
▶GWAS Catalog Trait Associations (2)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (2)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
bone tissue density
Kemp JP et al. “Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment.” Plos Genetics 10(6):e1004423 (2014)
Allele G
OR 0.20
p 1.0e-37
N 9,416
Large GWAS
multi-ancestry
body height
Schoeler T et al. “Participation bias in the UK Biobank distorts genetic associations and downstream analyses.” Nature Human Behaviour 7(7):1216-1227 (2023)
Allele A
OR 0.11
p 3.0e-10
N 283,749
Major Consortium StudyLarge 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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