rs3025039, VEGFA

N. diseases: 62
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Retinal Diseases
CUI: C0035309
Disease: Retinal Diseases
0.010 GeneticVariation BEFREE CC genotype and C allele of rs2010963 and TT genotype and T allele of rs3025039 were significantly over represented among PDR subjects compared to DNR group. 25956512 2015