rs1801282, PPARG

N. diseases: 131
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
0.050 GeneticVariation BEFREE To our knowledge, this is the first report of association analysis of p.Pro12Ala polymorphism in PPARγ in DR patients from India. 27427939 2017
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
0.050 GeneticVariation BEFREE Among 34 previous signals for DR, after controlling for multiple testing, no association was replicated in our meta-analyses. rs1571942 and rs12219125 at PLXDC2 locus showed nominally significant (<0.05) association with SDR in the same direction as previous report, as did rs1801282 in PPARG gene with MDR. 25487307 2015
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
0.050 GeneticVariation BEFREE The association of non-synonymous substitution polymorphism rs1801282 (c.34C>G, p.Pro12Ala) in exon 4 of the peroxisome proliferator activated receptor gamma gene with diabetic retinopathy (DR) has been reported inconsistently. 23559865 2013
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
0.050 GeneticVariation BEFREE The alanine variant of the Pro12Ala polymorphism of PPARgamma might be associated with decreased risk of DR in T2DM. 18077048 2008
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
0.050 GeneticVariation BEFREE The present study demonstrates that the AA genotype of the Gly482Ser polymorphism in the PPARGC1 gene might be a risk factor for diabetic retinopathy in the Slovene population (Caucasians) with type 2 diabetes (odds ratio 2.7, 95% confidence interval 1.0-6.8), whereas the Pro12Ala polymorphism of the PPARgamma gene failed to confer susceptibility to diabetic retinopathy. 15782399 2005