Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3025033
rs3025033
0.010 GeneticVariation BEFREE The frequencies of 3 VEGF gene SNPs were analyzed, 1 at the promoter site (rs699947, A-->C) and 2 intronic SNPs (rs2146323, A-->C, and rs3025033, A-->G), in relation to the risk of AMD, to choroidal neovascular (CNV) lesion size and configuration, and to the anatomic response to photodynamic therapy (PDT). 19896188

2010

dbSNP: rs3024997
rs3024997
0.010 GeneticVariation BEFREE One SNP (rs3024997) showed evidence of departure from Hardy-Weinberg equilibrium in only the AMD cases. 18079689

2007

dbSNP: rs141138308
rs141138308
0.010 GeneticVariation BEFREE In this study, we investigated the association between ApoE C112R/R158C single nucleotide polymorphisms (which determine the E2, E3, and E4 isoforms) and age-related macular degeneration (AMD), and the mechanism underlying the association. 16823865

2006

dbSNP: rs752907384
rs752907384
0.010 GeneticVariation BEFREE In this study, we investigated the association between ApoE C112R/R158C single nucleotide polymorphisms (which determine the E2, E3, and E4 isoforms) and age-related macular degeneration (AMD), and the mechanism underlying the association. 16823865

2006