rs3856806, PPARG

N. diseases: 41
Disease: Ischemic stroke ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
0.020 GeneticVariation BEFREE The effect of the PPARG rs1801282 G allele on ischemic stroke risk was enhanced in the presence of the rs38</span>56806 T allele (OR = 8.001 vs. 1.844). 31290457 2019
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
0.020 GeneticVariation BEFREE To explore the relationship between the genetic polymorphisms of PPARgamma (Pro12Ala, C1431T, and C-2821T) and the risk of ischemic stroke and to investigate whether these genetic polymorphisms of PPARgamma would modify the risk of ischemic stroke among patients with hypertension or diabetes. 19651920 2009