Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1799983
rs1799983
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 GeneticVariation BEFREE The meta-analysis showed that G894T is significantly associated with diabetic nephropathy and diabetes leading to severe nephropathy in type 2 diabetics and in East Asians, respectively. 19773668

2009

dbSNP: rs1799983
rs1799983
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 GeneticVariation BEFREE We genotyped three polymorphisms of eNOS (two SNPs: T-786C, G894T and one 27 VNTR) in T2DM patients with overt nephropathy (cases: n=320) and T2DM patients without overt nephropathy (controls: n=490), using validated PCR-RFLP assays. 23260854

2013

dbSNP: rs1799983
rs1799983
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 GeneticVariation BEFREE In contrast, we did not observe any association between the genotypes or alleles of G894T polymorphism with DR, hypertension, or nephropathy. 18079690

2007

dbSNP: rs1799983
rs1799983
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 GeneticVariation BEFREE These mutant genotypes were found to be associated with higher risk of nephropathy (-786T > C: OR: 5.5, 95%CI: 1.53-19.79; 894G > T: OR: 1.8, 95%CI: 1.03-3.16; Intron 4: OR: 6.23, 95%CI: 2.23-16.31). 18401556

2008

dbSNP: rs1799983
rs1799983
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 GeneticVariation BEFREE NOS3 894G>T polymorphism is associated with progression of kidney disease and cardiovascular morbidity in type 2 diabetic patients: NOS3 as a modifier gene for diabetic nephropathy? 24603156

2013

dbSNP: rs1799983
rs1799983
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 GeneticVariation BEFREE A total of 3793 patients (DN) and 3161 controls (diabetes without nephropathy) for 4b/a, 2654 patients and 1993 controls for G894T and 1348 patients and 1175 controls for T786C were included in our analysis. 21084433

2011

dbSNP: rs1799983
rs1799983
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 GeneticVariation BEFREE No associations between the -786T>C, the VNTR intron 4 a/b and the 894G>T (Glu298Asp) polymorphisms in the eNOS gene and renal disease were observed in type 2 diabetic Caucasian-Brazilians. 21255858

2011

dbSNP: rs1799983
rs1799983
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 GeneticVariation BEFREE The C allele for -786T>C and the T allele for 894G>T were significantly more frequent in diabetics with nephropathy than in diabetics without nephropathy (p<0.001; odds ratio [OR] and 95% confidence interval [CI] for the C allele=1.64 [1.24-2.17] and p<0.001; OR and 95% CI=1.7 [1.27-2.26] for the T allele). 22313046

2012

dbSNP: rs1799983
rs1799983
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 GeneticVariation BEFREE Endothelial nitric oxide synthase (eNOS) Glu298Asp single nucleotide polymorphism (SNP) genotype has been associated with a worse phenotype amongst patients with established heart failure and in patients with progression of their renal disease. 25612295

2015

dbSNP: rs1799983
rs1799983
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 GeneticVariation BEFREE The G894T polymorphism of the eNOS gene is associated with severity of renal disease. 19376104

2009

dbSNP: rs1799983
rs1799983
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 GeneticVariation BEFREE The aim of this study was to evaluate the possible association between six SNPs (A-5466C, T-3892C, A-240T, C1237T, G2215A and A2350G) of the ACE gene and two SNPs (T-786C and G894T) of the eNOS gene with lupus nephropathy in a northern Chinese population. 20540812

2010