rs1061170, CFH

N. diseases: 72
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Drusen
CUI: C1260959
Disease: Drusen
0.050 GeneticVariation BEFREE Factors associated with a 15-year incidence of medium drusen were assessed using discrete logistic regression models after adjusting for age, sex, smoking status, serum lipid levels, systemic and dietary factors, and CFH rs1061170 and ARMS2 rs10490924 polymorphisms. 25838066 2015
Drusen
CUI: C1260959
Disease: Drusen
0.050 GeneticVariation BEFREE Current smoking at baseline predicted higher reticular drusen incidence (OR 2.1, 95% CI 1.0-4.5) after adjusting for age, sex, CFH-rs1061170 and ARMS2-rs10490924 polymorphisms. 24332537 2014
Drusen
CUI: C1260959
Disease: Drusen
0.050 GeneticVariation BEFREE A FH Tyr402His polymorphism in SCR-7 is associated with age-related macular degeneration (AMD) and leads to deposition of complement in drusen. 20711705 2010
Drusen
CUI: C1260959
Disease: Drusen
0.050 GeneticVariation BEFREE This supports an autosomal-recessive disease model in which individuals who carry a CFH mutation on one allele and the Tyr402His variant on the other allele develop drusen. 18252232 2008
Drusen
CUI: C1260959
Disease: Drusen
0.050 GeneticVariation BEFREE The CFH Y402H polymorphism showed a genotype-phenotype association for some drusen features. 18211923 2008