CELF2, CUGBP Elav-like family member 2, 10659

N. diseases: 58; N. variants: 22
Disease: Adverse effects, not elsewhere classified ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs192238733
rs192238733
Entrez Id: 10659
Gene Symbol: CELF2
CELF2
CUI: C0869220
Disease:
Adverse effects, not elsewhere classified 		A 0.700 GeneticVariation GWASCAT Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health records. 30420678 2019