rs7630163

This is a intron variant variant in the CPN2 gene.

GWAS Catalog Trait Associations (1)

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

protein measurement

Pietzner M et al. Mapping the proteo-genomic convergence of human diseases. Science (new York, N.y.) 374(6569):eabj1541 (2021)
Allele A
OR 0.15
p 2.0e-26
N 10,708
Large GWAS
European

About CPN2

Predicted to enable enzyme regulator activity. Predicted to be involved in protein stabilization. Located in blood microparticle and extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]

View all CPN2 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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