Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2010963
rs2010963
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.030 GeneticVariation BEFREE Genomic DNA was isolated from whole blood for the analysis of <i>VEGF-A</i> (rs2010963, 1570360, rs699947), <i>ICAM-1</i> (rs5498, rs1799969) SNPs and from tumor tissue for the detection of genomic variants in <i>KRAS</i>, <i>NRAS</i>, <i>BRAF</i> genes. 31752122

2019

dbSNP: rs2010963
rs2010963
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.030 GeneticVariation BEFREE Moreover, VEGF rs699947 and rs2010963 polymorphisms may serve as genetic biomarkers of poor collateral circulation after myocardial ischemia. 30317903

2018

dbSNP: rs2010963
rs2010963
CUI: C0017638
Disease: Glioma
Glioma
0.030 GeneticVariation BEFREE Also, the VEGF polymorphisms rs3024994, rs2010963, and particularly the homozygous carriers of rs1005230 were associated with a worse prognosis for glioma and glioblastoma. 29584591

2018

dbSNP: rs2010963
rs2010963
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.030 GeneticVariation BEFREE Besides, rs3025039 polymorphism was significantly correlated with the number of affected coronary arteries, while rs699947 and rs2010963 polymorphisms were significantly correlated with poor collateral circulation in CHD patients. 30317903

2018

dbSNP: rs2010963
rs2010963
Conventional (Clear Cell) Renal Cell Carcinoma
0.030 GeneticVariation BEFREE As to rs1570360 or rs2010963, we did not observe any relationship between the two polymorphisms and RCC risk in our study. 28356760

2017

dbSNP: rs2010963
rs2010963
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.030 GeneticVariation BEFREE In conclusion, our findings suggest that VEGFA rs699947 C>A, rs3025039 C>T and rs2010963 G>C polymorphisms are risk factors for CHD. 28430629

2017

dbSNP: rs2010963
rs2010963
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.030 GeneticVariation BEFREE Our results indicate that VEGF (rs2010963) polymorphism and CTC haplotype of the VEGF SNPs (rs699947, rs833061, and rs2010963) confer an increased risk of psoriasis in the South Indian Tamil population. 28803785

2017

dbSNP: rs2010963
rs2010963
Conventional (Clear Cell) Renal Cell Carcinoma
0.030 GeneticVariation BEFREE Our meta-analysis suggested that there may be a relationship between the VEGF rs2010963, rs3025039 and rs699947 polymorphisms and RCC susceptibility. 28562357

2017

dbSNP: rs2010963
rs2010963
CUI: C0017638
Disease: Glioma
Glioma
0.030 GeneticVariation BEFREE The haplotype analysis demonstrated that two SNPs of VEGF [rs3025039 (C>T), rs2010963 (G>C)] could elevate the susceptibility to a glioma in the homozygous model [odds ratio (OR) = 3.13 (95% confidence interval (CI) 1.30-7.49, P = 0.007) and OR = 1.58 (95% CI 1.07-2.34, P = 0.022), respectively], dominant model [OR = 1.38 (95% CI 1.04-1.84, P = 0.025) and OR = 1.32 (95% CI 1.01-1.72, P = 0.043), respectively], and allelic model [OR = 1.43 (95% CI 1.11-1.84, P = 0.005) and OR = 1.24 (95% CI 1.04-1.50, P = 0.019), respectively]. 26093379

2016

dbSNP: rs2010963
rs2010963
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.030 GeneticVariation BEFREE Angiotensin converting enzyme insertion/deletion (I/D) (rs4646994) and Vegf polymorphism (+405G/C; rs2010963) in type II diabetic patients: Association with the risk of coronary artery disease. 24505095

2015

dbSNP: rs2010963
rs2010963
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.030 GeneticVariation BEFREE Angiotensin converting enzyme insertion/deletion (I/D) (rs4646994) and Vegf polymorphism (+405G/C; rs2010963) in type II diabetic patients: Association with the risk of coronary artery disease. 24505095

2015

dbSNP: rs2010963
rs2010963
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.030 GeneticVariation BEFREE The aim of this meta-analysis was to investigate large-scale evidence to determine the degree to which four common VEGF polymorphisms (+405C>G [dbSNP: rs2010963], -460T>C [dbSNP: rs833061], -2578C>A [dbSNP: rs699947], and -1154G>A [dbSNP: rs1570360]) are associated with susceptibility to psoriasis. 24678886

2014

dbSNP: rs2010963
rs2010963
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.030 GeneticVariation BEFREE After stratifying by tumor molecular subtype, SNP associations observed for colon cancer were: VEGFA rs2010963 with CIMP+ colon tumors; FLT1 rs4771249 and rs7987649 with TP53; FLT1 rs3751397, rs7337610, rs7987649, and rs9513008 and KDR rs10020464, rs11941492, and rs12498529 with MSI+ and CIMP+/KRAS2-mutated tumors. 23794399

2014

dbSNP: rs2010963
rs2010963
Conventional (Clear Cell) Renal Cell Carcinoma
0.030 GeneticVariation BEFREE Our results indicate that VEGFA rs2010963 and VEGFR3 rs448012 are associated with risk of ccRCC. 25239121

2014

dbSNP: rs2010963
rs2010963
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.030 GeneticVariation BEFREE Blood and tumor tissue from 83 patients with NSCLC were examined for VEGF -460T/C (rs833061) and VEGF +405G/C (rs2010963) SNPs using the SNaPshot method. 23064377

2013

dbSNP: rs2010963
rs2010963
CUI: C0017638
Disease: Glioma
Glioma
0.030 GeneticVariation BEFREE In the single-locus analysis, we found that rs2010963 (G+405C, G-634C) [odds ratio (OR) = 1.29; 95% confidence interval (CI) = 1.04-1.58; GC/CC vs. GG] and rs3025030 (OR = 2.21; 95% CI = 1.18-4.14; CC vs. GG/GC) were associated with increased risk for glioma, and rs3024994 (OR = 0.66; 95% CI = 0.47-0.94; CT/TT vs. CC) was associated with reduced glioma risk, albeit insignificant after Bonferroni correction for multiple comparisons. 20209496

2011

dbSNP: rs2010963
rs2010963
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.030 GeneticVariation BEFREE We examined two VEGF polymorphisms, including +405 C/G (rs2010963) and -2578C/A (rs699947), to assess their relation to the extent of coronary atherosclerosis. 20489684

2010

dbSNP: rs2010963
rs2010963
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
0.020 GeneticVariation BEFREE Our study shows for the first time that the rs2010963 polymorphism may be associated with a risk of PCOS in Northern Chinese women. 30935253

2019

dbSNP: rs2010963
rs2010963
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.020 GeneticVariation BEFREE Also, the VEGF polymorphisms rs3024994, rs2010963, and particularly the homozygous carriers of rs1005230 were associated with a worse prognosis for glioma and glioblastoma. 29584591

2018

dbSNP: rs2010963
rs2010963
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
0.020 GeneticVariation BEFREE Also, the VEGF polymorphisms rs3024994, rs2010963, and particularly the homozygous carriers of rs1005230 were associated with a worse prognosis for glioma and glioblastoma. 29584591

2018

dbSNP: rs2010963
rs2010963
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
0.020 GeneticVariation BEFREE As to rs1570360 or rs2010963, we did not observe any relationship between the two polymorphisms and RCC risk in our study. 28356760

2017

dbSNP: rs2010963
rs2010963
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
0.020 GeneticVariation BEFREE Our meta-analysis suggested that there may be a relationship between the VEGF rs2010963, rs3025039 and rs699947 polymorphisms and RCC susceptibility. 28562357

2017

dbSNP: rs2010963
rs2010963
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.020 GeneticVariation BEFREE We found that the VEGF rs2010963 CG + GG genotypes had a significantly increased risk of hand-foot syndrome, and the ABCB1 rs1045642 CT + TT genotypes had an increased risk of high blood pressure. 26830973

2016

dbSNP: rs2010963
rs2010963
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
0.020 GeneticVariation BEFREE Increased and reduced PCOS risk was seen with rs3025020 and rs2010963 genotypes, respectively. 27846231

2016

dbSNP: rs2010963
rs2010963
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.020 GeneticVariation BEFREE Also, adjusted ORs in the presence of normolipidemia and the absence of history of hypertension for the risk of CAD in the either ACE(rs4646994) D allele or VGEF(rs2010963)-G alleles were 2.08 (p=0.004) and 1.75 (p=0.024), respectively. 24505095

2015