Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1061170
rs1061170
CFH
0.020 GeneticVariation BEFREE Molecular Mechanisms of Macular Degeneration Associated with the Complement Factor H Y402H Mutation. 30616835

2019
dbSNP: rs1061170
rs1061170
CFH
0.020 GeneticVariation BEFREE Differential binding to C-reactive protein, thus, does not explain association of the Y402H polymorphism with macular degeneration. 18786923

2008