Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4938723
rs4938723
Entrez Id: 54766;407041;407042;728196
Gene Symbol: BTG4;MIR34B;MIR34C;LOC728196
BTG4;MIR34B;MIR34C;LOC728196
CUI: C1956346
Disease:
Coronary Artery Disease
0.010 GeneticVariation BEFREE Our findings suggest that the pri-miR-34b/c rs4938723 polymorphism is associated with CAD susceptibility in the Chinese Han population. 31499476 2019