Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs757537938
rs757537938
0.030 GeneticVariation BEFREE Although the E318D and L9H variants have shown association with AMD in previous studies, the findings were not in agreement. 18806293

2009

dbSNP: rs757537938
rs757537938
0.030 GeneticVariation BEFREE Three SNPs in CC2 and CFB were strongly associated with decreased risk of AMD in the case-control data set (CC2 E318D: P = 0.02; CC2 rs547154: P = 9 x 10(-6); and CFB R32Q P = 2 x 10(-5)). 17576744

2007

dbSNP: rs757537938
rs757537938
0.030 GeneticVariation BEFREE The L9H variant of BF and the E318D variant of C2 (H10), as well as a variant in intron 10 of C2 and the R32Q variant of BF (H7), confer a significantly reduced risk of AMD (odds ratio = 0.45 and 0.36, respectively). 16518403

2006