Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs699947
rs699947
0.060 GeneticVariation BEFREE The VEGF gene SNPs analyzed with regard to DR susceptibility were rs2010963 (G > C), rs833061 (T > C), rs699947 (C > A), rs3025039 (C > T) and rs1570360 (G > A). 27613596

2017

dbSNP: rs699947
rs699947
0.060 GeneticVariation BEFREE After adjustment for covariates, significant association of DR remained with the homozygous genotype of the minor allele for the SNPs rs699947 (odds ratio [OR] = 3.54, 95% confidence interval [CI]: 1.12-11.19), rs833061 (OR = 3.72, 95% CI: 1.17-11.85), rs13207351 (OR = 3.76, 95% CI: 1.21-11.71), and rs2146323 (OR = 2.8, 95% CI: 1.46-5.37) in the VEGF gene as well as the SNP rs2071559 (OR = 1.62, 95% CI: 1.08-2.41) in the KDR gene. 24623964

2014

dbSNP: rs699947
rs699947
0.060 GeneticVariation BEFREE No evidence of association was observed between -2578 A/C (rs699947), +405C/G (rs2010963), +936C/T (rs3025039), and DR risk under stringent Bonferroni's correction. 24534217

2014

dbSNP: rs699947
rs699947
0.060 GeneticVariation BEFREE Our meta-analysis confirmed the significant association between rs699947 polymorphism and DR after exclusion of outliers, and rs2010963 polymorphism might be not associated with DR. 24131746

2013

dbSNP: rs699947
rs699947
0.060 GeneticVariation BEFREE After adjusting for covariates, a significant association of DR was observed with the homozygous genotype of the minor allele for promoter SNPs rs699947 (odds ratio (OR)=3.54, 95% confidence interval (CI): 1.12-11.19), rs833061 (OR=3.72, 95% CI: 1.17-11.85) and rs13207351 (OR=3.76, 95% CI: 1.21-11.71). 22162628

2011

dbSNP: rs699947
rs699947
0.060 GeneticVariation BEFREE We found a significant association between the A allele at rs699947 with DR (odds ratio = 1.84 (95% confidence interval = 1.28-2.66); P = 0.001 vs. noDR). 20444917

2010

dbSNP: rs2146323
rs2146323
0.040 GeneticVariation BEFREE The allelic distribution of VEGF-A rs2146323 polymorphism tended to be associated with the severity of DRP (p = 0.069). 29030794

2018

dbSNP: rs2010963
rs2010963
0.040 GeneticVariation BEFREE The VEGF gene SNPs analyzed with regard to DR susceptibility were rs2010963 (G > C), rs833061 (T > C), rs699947 (C > A), rs3025039 (C > T) and rs1570360 (G > A). 27613596

2017

dbSNP: rs833061
rs833061
0.040 GeneticVariation BEFREE The T allele in rs3025039 and the C allele in rs833061 are associated with increased DR susceptibility. 27613596

2017

dbSNP: rs2010963
rs2010963
0.040 GeneticVariation BEFREE We found the frequencies of the CC, CG, and GG genotype of the rs2010963 polymorphism were 15.09%, 47.14%, and 37.74% in DR and 12.90%, 19.35%, and 67.74% in DNR, respectively (p = 0.0205). 27648002

2016

dbSNP: rs2146323
rs2146323
0.040 GeneticVariation BEFREE Our meta-analysis confirmed the association between the VEGF rs2146323 polymorphism and the risk of DR. 26553067

2015

dbSNP: rs2010963
rs2010963
0.040 GeneticVariation BEFREE No evidence of association was observed between -2578 A/C (rs699947), +405C/G (rs2010963), +936C/T (rs3025039), and DR risk under stringent Bonferroni's correction. 24534217

2014

dbSNP: rs2146323
rs2146323
0.040 GeneticVariation BEFREE After adjustment for covariates, significant association of DR remained with the homozygous genotype of the minor allele for the SNPs rs699947 (odds ratio [OR] = 3.54, 95% confidence interval [CI]: 1.12-11.19), rs833061 (OR = 3.72, 95% CI: 1.17-11.85), rs13207351 (OR = 3.76, 95% CI: 1.21-11.71), and rs2146323 (OR = 2.8, 95% CI: 1.46-5.37) in the VEGF gene as well as the SNP rs2071559 (OR = 1.62, 95% CI: 1.08-2.41) in the KDR gene. 24623964

2014

dbSNP: rs833061
rs833061
0.040 GeneticVariation BEFREE After adjustment for covariates, significant association of DR remained with the homozygous genotype of the minor allele for the SNPs rs699947 (odds ratio [OR] = 3.54, 95% confidence interval [CI]: 1.12-11.19), rs833061 (OR = 3.72, 95% CI: 1.17-11.85), rs13207351 (OR = 3.76, 95% CI: 1.21-11.71), and rs2146323 (OR = 2.8, 95% CI: 1.46-5.37) in the VEGF gene as well as the SNP rs2071559 (OR = 1.62, 95% CI: 1.08-2.41) in the KDR gene. 24623964

2014

dbSNP: rs833061
rs833061
0.040 GeneticVariation BEFREE A significant relationship between VEGF+936C/T (rs3025039) polymorphism and DR was found in a recessive model (OR = 3.19, 95% CI = 1.20-8.41, and P(z) = 0.01) in Asian and overall populations, while a significant association was also found between -460T/C (rs833061) polymorphism and DR risk under a recessive model (OR = 2.12, 95% CI = 1.12-4.01, and P(z) = 0.02).CONCLUSIONS. 24868559

2014

dbSNP: rs2010963
rs2010963
0.040 GeneticVariation BEFREE Our meta-analysis confirmed the significant association between rs699947 polymorphism and DR after exclusion of outliers, and rs2010963 polymorphism might be not associated with DR. 24131746

2013

dbSNP: rs2146323
rs2146323
0.040 GeneticVariation BEFREE A significant association of DR was also observed with haplotype ACA, as defined by minor alleles of promoter SNPs rs699947, rs833061, and rs13207351 (OR=1.52, 95% CI: 1.03-2.24), and haplotype GAA, as defined by SNPs rs2010963, rs833069, and rs2146323 (OR=1.62, 95% CI: 1.08-2.41). 22162628

2011

dbSNP: rs833061
rs833061
0.040 GeneticVariation BEFREE After adjusting for covariates, a significant association of DR was observed with the homozygous genotype of the minor allele for promoter SNPs rs699947 (odds ratio (OR)=3.54, 95% confidence interval (CI): 1.12-11.19), rs833061 (OR=3.72, 95% CI: 1.17-11.85) and rs13207351 (OR=3.76, 95% CI: 1.21-11.71). 22162628

2011

dbSNP: rs3025039
rs3025039
0.030 GeneticVariation BEFREE The T allele in rs3025039 and the C allele in rs833061 are associated with increased DR susceptibility. 27613596

2017

dbSNP: rs3025039
rs3025039
0.030 GeneticVariation BEFREE A significant relationship between VEGF+936C/T (rs3025</span>039) polymorphism and DR was found in a recessive model (OR = 3.19, 95% CI = 1.20-8.41, and P(z) = 0.01) in Asian and overall populations, while a significant association was also found between -460T/C (rs833061) polymorphism and DR risk under a recessive model (OR = 2.12, 95% CI = 1.12-4.01, and P(z) = 0.02).CONCLUSIONS. 24868559

2014

dbSNP: rs3025039
rs3025039
0.030 GeneticVariation BEFREE No evidence of association was observed between -2578 A/C (rs699947), +405C/G (rs2010963), +936C/T (rs3025039), and DR risk under stringent Bonferroni's correction. 24534217

2014

dbSNP: rs833069
rs833069
0.020 GeneticVariation BEFREE However, the VEGF-A rs833069 gene polymorphism has a clear association with the severity of diabetic retinopathy. 29030794

2018

dbSNP: rs13207351
rs13207351
0.020 GeneticVariation BEFREE After adjustment for covariates, significant association of DR remained with the homozygous genotype of the minor allele for the SNPs rs699947 (odds ratio [OR] = 3.54, 95% confidence interval [CI]: 1.12-11.19), rs833061 (OR = 3.72, 95% CI: 1.17-11.85), rs13207351 (OR = 3.76, 95% CI: 1.21-11.71), and rs2146323 (OR = 2.8, 95% CI: 1.46-5.37) in the VEGF gene as well as the SNP rs2071559 (OR = 1.62, 95% CI: 1.08-2.41) in the KDR gene. 24623964

2014

dbSNP: rs13207351
rs13207351
0.020 GeneticVariation BEFREE After adjusting for covariates, a significant association of DR was observed with the homozygous genotype of the minor allele for promoter SNPs rs699947 (odds ratio (OR)=3.54, 95% confidence interval (CI): 1.12-11.19), rs833061 (OR=3.72, 95% CI: 1.17-11.85) and rs13207351 (OR=3.76, 95% CI: 1.21-11.71). 22162628

2011

dbSNP: rs833069
rs833069
0.020 GeneticVariation BEFREE A significant association of DR was also observed with haplotype ACA, as defined by minor alleles of promoter SNPs rs699947, rs833061, and rs13207351 (OR=1.52, 95% CI: 1.03-2.24), and haplotype GAA, as defined by SNPs rs2010963, rs833069, and rs2146323 (OR=1.62, 95% CI: 1.08-2.41). 22162628

2011