Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3791
Gene Symbol: KDR
KDR
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		0.070 Biomarker BEFREE VEGF/VEGFR2 blockade does not cause retinal atrophy in AMD-relevant models. 29769445

2018
Entrez Id: 3791
Gene Symbol: KDR
KDR
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		0.070 GeneticVariation BEFREE The CATT and IVAN data do not support a pharmacogenetic association between the 2 VEGFR2 SNPs, rs4576072 and rs6828477, and change in VA in response to anti-VEGF therapy in patients with neovascular AMD. 26028346

2015
Entrez Id: 3791
Gene Symbol: KDR
KDR
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		0.070 GeneticVariation BEFREE Polymorphisms in the VEGFR2/KDR gene significantly influence visual outcome in patients receiving ranibizumab treatment for neovascular AMD. 24365177

2014
Entrez Id: 3791
Gene Symbol: KDR
KDR
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		0.070 GeneticVariation BEFREE Predictive value of VEGF A and VEGFR2 polymorphisms in the response to intravitreal ranibizumab treatment for wet AMD. 24522370

2014
Entrez Id: 3791
Gene Symbol: KDR
KDR
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		0.070 GeneticVariation BEFREE VEGF A (rs699947 and rs833061) and VEGFR2 (rs2071559) gene polymorphisms are not associated with AMD susceptibility in a Spanish population. 23971975

2013
Entrez Id: 3791
Gene Symbol: KDR
KDR
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		0.070 GeneticVariation BEFREE Genotypes of polymorphisms in known AMD susceptibility loci (CFH, CFB, HTRA1, AMRS2, and VEGFA) as well as not yet reported AMD-associated genes (KDR, LRP5, and FZD4) were determined, and their frequencies were compared. 21282580

2011
Entrez Id: 3791
Gene Symbol: KDR
KDR
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		0.070 GeneticVariation BEFREE A single rare haplotype in the VEGFR-2 gene was associated with the presence of neovascular AMD (p=0.034). 20019880

2009