CELF2, CUGBP Elav-like family member 2, 10659

N. diseases: 58; N. variants: 22
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11256837
rs11256837
Entrez Id: 10659
Gene Symbol: CELF2
CELF2
CUI: C0871470
Disease:
Systolic Pressure
A 0.700 GeneticVariation GWASCAT Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. 30578418 2019