rs12219125, None

N. diseases: 2
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
0.810 GeneticVariation BEFREE <b>Results:</b> The SNPs rs9362054 near the <i>CEP162</i> gene and rs4462262 near the <i>UBE2D1</i> gene were associated with DR (OR = 1.66, <i>p</i> = 0.001; OR = 1.37, <i>p</i> = 0.031; respectively), and rs12219125 near the <i>PLXDC2</i> gene was associated (suggestive) with CAD (OR = 2.26, <i>p</i> = 0.034). 31130920 2019
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
0.810 GeneticVariation GWASDB Genome-wide association study of diabetic retinopathy in a Taiwanese population. 21310492 2011
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
0.810 GeneticVariation GWASCAT Genome-wide association study of diabetic retinopathy in a Taiwanese population. 21310492 2011
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
0.010 GeneticVariation BEFREE <b>Results:</b> The SNPs rs9362054 near the <i>CEP162</i> gene and rs4462262 near the <i>UBE2D1</i> gene were associated with DR (OR = 1.66, <i>p</i> = 0.001; OR = 1.37, <i>p</i> = 0.031; respectively), and rs12219125 near the <i>PLXDC2</i> gene was associated (suggestive) with CAD (OR = 2.26, <i>p</i> = 0.034). 31130920 2019