Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1883414
rs1883414
HLA-DPB2
0.800 GeneticVariation GWASDB Genome-wide association study identifies susceptibility loci for IgA nephropathy. 21399633

2011
dbSNP: rs1883414
rs1883414
HLA-DPB2
0.800 GeneticVariation GWASCAT Genome-wide association study identifies susceptibility loci for IgA nephropathy. 21399633

2011
dbSNP: rs2412971
rs2412971
HORMAD2
0.800 GeneticVariation GWASDB Genome-wide association study identifies susceptibility loci for IgA nephropathy. 21399633

2011
dbSNP: rs2412971
rs2412971
HORMAD2
0.800 GeneticVariation GWASCAT Genome-wide association study identifies susceptibility loci for IgA nephropathy. 21399633

2011
dbSNP: rs6677604
rs6677604
CFH
0.800 GeneticVariation GWASCAT Genome-wide association study identifies susceptibility loci for IgA nephropathy. 21399633

2011
dbSNP: rs6677604
rs6677604
CFH
0.800 GeneticVariation GWASDB Genome-wide association study identifies susceptibility loci for IgA nephropathy. 21399633

2011
dbSNP: rs9275596
rs9275596 		0.800 GeneticVariation GWASCAT Genome-wide association study identifies susceptibility loci for IgA nephropathy. 21399633

2011
dbSNP: rs9275596
rs9275596 		0.800 GeneticVariation GWASDB Genome-wide association study identifies susceptibility loci for IgA nephropathy. 21399633

2011
dbSNP: rs9357155
rs9357155
PSMB8
0.800 GeneticVariation GWASCAT Genome-wide association study identifies susceptibility loci for IgA nephropathy. 21399633

2011
dbSNP: rs9357155
rs9357155
PSMB8
0.800 GeneticVariation GWASDB Genome-wide association study identifies susceptibility loci for IgA nephropathy. 21399633

2011
dbSNP: rs3115573
rs3115573 		0.800 GeneticVariation GWASCAT HLA has strongest association with IgA nephropathy in genome-wide analysis. 20595679

2010
dbSNP: rs3115573
rs3115573 		0.800 GeneticVariation GWASDB HLA has strongest association with IgA nephropathy in genome-wide analysis. 20595679

2010
dbSNP: rs2856717
rs2856717 		0.700 GeneticVariation GWASDB Genome-wide association study identifies susceptibility loci for IgA nephropathy. 21399633

2011
dbSNP: rs9275224
rs9275224 		0.700 GeneticVariation GWASDB Genome-wide association study identifies susceptibility loci for IgA nephropathy. 21399633

2011
dbSNP: rs9275424
rs9275424 		0.700 GeneticVariation GWASDB Genome-wide association study identifies susceptibility loci for IgA nephropathy. 21399633

2011
dbSNP: rs1799983
rs1799983
NOS3
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: rs699
rs699
AGT
0.100 GeneticVariation BEFREE Genetic variants of ACE (Insertion/Deletion) and AGT (M268T) genes in patients with diabetes and nephropathy. 24737640

2014
dbSNP: rs1799983
rs1799983
NOS3
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
NOS3
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: rs699
rs699
AGT
0.100 GeneticVariation BEFREE To assess the antiproteinuric response to multifactorial treatment based on high doses of angiotensin II receptor antagonists (ARBs) (olmesartan) in patients with non-diabetic proteinuric nephropathies, according to three renin-angiotensin system (RAS) polymorphisms: insertion/deletion of the angiotensin converting enzyme (ACE) gene, the angiotensinogen gene M235T and the angiotensin II type 1 receptor (AT1R) A1166C. 24241364

2013
dbSNP: rs1799983
rs1799983
NOS3
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
NOS3
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
NOS3
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: rs699
rs699
AGT
0.100 GeneticVariation BEFREE Association of the angiotensinogen M235T and APO E gene polymorphisms in Turkish type 2 diabetic patients with and without nephropathy. 21500980

2011
dbSNP: rs1799983
rs1799983
NOS3
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