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 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
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