Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1799983
rs1799983
0.050 GeneticVariation BEFREE In this case-control study, the relationship of the -786T/C, the VNTR intron 4 a/b and the 894G/T (Glu298Asp) polymorphisms in the eNOS gene with the presence or severity of diabetic retinopathy was analyzed in 630 Caucasian-Brazilians with type 2 diabetes (434 with and 196 without diabetic retinopathy). 22017289

2012

dbSNP: rs1799983
rs1799983
0.050 GeneticVariation BEFREE In both the cohorts, consistently lower prevalence and decreased risk of DR was observed in patients with ba, aa and ba + aa genotype of 27VNTR (a/b), C-a-G and C-a-T haplotype (allele of T-786C, 27VNTR a/b and G894T) carrying "C" allele of T-786C and "a" allele of 27VNTR (a/b). 23085930

2012

dbSNP: rs1799983
rs1799983
0.050 GeneticVariation BEFREE However, the G894T polymorphism does not appear to influence the development of DR. 22506535

2012

dbSNP: rs1799983
rs1799983
0.050 GeneticVariation BEFREE Lower prevalence of mutant 4a (P = 0.011), and heterozygous 4b/4a (P = 0.042) were seen in the DR compared to the DWR groups; the allele and genotype distribution of the Glu298Asp and T-786C polymorphisms were comparable between DR and DWR groups. 17973941

2008

dbSNP: rs1799983
rs1799983
0.050 GeneticVariation BEFREE We studied three eNOS genetic polymorphisms: a single nucleotide polymorphism in the promoter region (T(-786)C), in exon 7 (Glu298Asp), and a variable number of tandem repeats in intron 4 (b/a) in 103 healthy controls, and in 170 patients with T2DM (without DR, N=114; with DR, N=56). 16581274

2006

dbSNP: rs869109213
rs869109213
0.020 GeneticVariation BEFREE The Role of Genetic Variants (rs869109213 and rs2070744) Of the <i>eNOS</i> Gene and <i>Bgl</i>II in the α<sub>2</sub> Subunit of the α<sub>2</sub>β<sub>1</sub> Integrin Gene in Diabetic Retinopathy in a Tunisian Population. 31257963

2019

dbSNP: rs869109213
rs869109213
0.020 GeneticVariation BEFREE We found a significant association between the genotypes of NOS3 rs869109213 polymorphism and the risk of DR in the co-dominant model (4a4b genotype; 1.99-fold increased risk [1.09-3.65]; 95% confidence interval [CI]; p = 0.02), co-dominant model (4a4a genotype; 4.16-fold increased risk [1.03-16.74]; 95% CI; p = 0.04), and dominant model (4a4a and 4a4b genotypes; 2.22-fold increased risk [1.26-3.92]; 95% CI; p = 0.01) compared to the 4b4b genotype. 28817788

2018

dbSNP: rs2070744
rs2070744
0.010 GeneticVariation BEFREE The Role of Genetic Variants (rs869109213 and rs2070744) Of the <i>eNOS</i> Gene and <i>Bgl</i>II in the α<sub>2</sub> Subunit of the α<sub>2</sub>β<sub>1</sub> Integrin Gene in Diabetic Retinopathy in a Tunisian Population. 31257963

2019

dbSNP: rs1549758
rs1549758
0.010 GeneticVariation BEFREE These findings, supported by previous associations between eNOS4b/a polymorphism and DR, suggest that T-786C and C774T eNOS polymorphisms affect the onset pattern of severe DR. 15890549

2005