Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1267969615
rs1267969615
ACE
0.100 GeneticVariation BEFREE We investigated the gender differences in the effect of ACE I/D and AGT M235T polymorphisms on the prognosis of diabetic nephropathy (DN). 18849600

2009

dbSNP: rs1267969615
rs1267969615
ACE
0.100 GeneticVariation BEFREE We investigated the relationship of the ACE insertion/deletion (I/D) and AGT M235T</span> gene polymorphisms in Turkish patients with type 2 diabetes mellitus (DM) with and without diabetic nephropathy. 18413162

2008

dbSNP: rs1267969615
rs1267969615
ACE
0.100 GeneticVariation BEFREE The impact of polymorphisms in the genes coding for angiotensinogen (M235T), ACE (ID), and angiotensin II type 1 receptor (A(1166)-->C) on decline in GFR and doubling of s-creatinine or development of ESRD in patients with type 1 diabetes and diabetic nephropathy (DN) was tested. 14569094

2003

dbSNP: rs1267969615
rs1267969615
ACE
0.100 GeneticVariation BEFREE Conflicting results on the relationship between M235T polymorphism of angiotensinogen (AGT) gene and diabetic nephropathy are reported in the literature, probably due to the small number of subjects, to different inclusion criteria and the different genotype analysis methods used. 12270765

2002

dbSNP: rs1267969615
rs1267969615
ACE
0.100 GeneticVariation BEFREE A substitution (M235T) polymorphism in angiotensinogen (AGT) may interact with ACE I/D polymorphism for the risk of diabetic nephropathy, but their prognostic values have to be established by follow-up studies. 11181802

2001

dbSNP: rs1267969615
rs1267969615
ACE
0.100 GeneticVariation BEFREE Our study revealed RAS genes, ACE and AGT-M235T but not AGT-T174M, AGTR1 or REN genotypes, as contributing factors for DN in type 2 diabetes mellitus in Chinese. 11776100

2000

dbSNP: rs1267969615
rs1267969615
ACE
0.100 GeneticVariation BEFREE Therefore, we investigated the interaction between long-term glycaemic control and three polymorphisms in the genes coding for AGTR1 (A1166-->C), angiotensin converting enzyme (ACE/ID) and angiotensinogen (M235T) on risk of developing diabetic nephropathy. 10907125

2000

dbSNP: rs1267969615
rs1267969615
ACE
0.100 GeneticVariation BEFREE The data do not support a role of ACE (DD/II) or Atg M235T polymorphism in the development of diabetic nephropathy in Chinese patients with type II diabetes, and no synergistic effect was found between them. 10352194

1999

dbSNP: rs1267969615
rs1267969615
ACE
0.100 GeneticVariation BEFREE Furthermore, an M235T variant of the angiotensinogen (AGT) gene has been associated with hypertension, an important risk factor for the development and progression of diabetic nephropathy. 9049480

1997

dbSNP: rs1267969615
rs1267969615
ACE
0.100 GeneticVariation BEFREE These results suggested that ACE I/D polymorphism, but not AGN M235T polymorphism, is a possible genetic risk factor for diabetic nephropathy in Japanese NIDDM patients. 8596493

1996

dbSNP: rs1267969615
rs1267969615
ACE
0.100 GeneticVariation BEFREE We have examined the angiotensin converting enzyme insertion/deletion polymorphism and angiotensinogen methionine 235 threonine polymorphism in a large cohort of Caucasian patients with IDDM and diabetic nephropathy. 8877296

1996

dbSNP: rs1799752
rs1799752
ACE
0.020 GeneticVariation BEFREE Minor allele frequency of rs1800764 was higher in DN patients than DWN patients or healthy controls, and minor allele frequency of rs1799752 was higher in DN than DWN patients. 19787680

2009

dbSNP: rs1799752
rs1799752
ACE
0.020 GeneticVariation BEFREE In the case-control analysis, the rs1800764-C, rs4311-T, Insertion/deletion (I/D or rs1799752)-D, rs4366-G, and rs12449782-G alleles were associated with an increased risk for DN, homogeneously across populations, with allelic odds ratios of 1.11 (95% confidence interval 1.00 to 1.22), 1.18 (1.04 to 1.33), 1.13 (1.02 to 1.23), 1.10 (0.99 to 1.20), and 1.12 (1.01 to 1.23), respectively. 17376814

2007

dbSNP: rs1341633213
rs1341633213
ACE
0.010 GeneticVariation BEFREE In this study, a case-control study was carried out to investigate the effects of 7 SNPs in ACE gene and 2 SNPs in eNOS gene in the development of DN in Northern China.7 SNPs including A240T, A2350G, A5466C, A2215G, T3892C, C1237T and C3409T of ACE gene and 2 SNPs (G894T and T786C) of eNOS gene were genotyped by polymerase chain reaction restriction fragment length polymorphism method. 25227524

2015

dbSNP: rs4311
rs4311
ACE
0.010 GeneticVariation BEFREE In the case-control analysis, the rs1800764-C, rs4311-T, Insertion/deletion (I/D or rs1799752)-D, rs4366-G, and rs12449782-G alleles were associated with an increased risk for DN, homogeneously across populations, with allelic odds ratios of 1.11 (95% confidence interval 1.00 to 1.22), 1.18 (1.04 to 1.33), 1.13 (1.02 to 1.23), 1.10 (0.99 to 1.20), and 1.12 (1.01 to 1.23), respectively. 17376814

2007

dbSNP: rs4366
rs4366
ACE
0.010 GeneticVariation BEFREE Haplotype analysis further demonstrated that the haplotype defined by the D, rs4366_G and rs12449782_G alleles was associated with a greater risk for DN. 17376814

2007

dbSNP: rs1157043147
rs1157043147
ACE
0.010 GeneticVariation BEFREE Our results suggest that TGF-beta T869C (Leu 10Pro) gene polymorphism is associated with DMN in Chinese. 12675860

2003