Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1061170
rs1061170
CFH
0.060 GeneticVariation BEFREE Complement factor H Y402H gene polymorphism and coronary heart disease susceptibility: a meta-analysis. 20127520

2011
dbSNP: rs1061170
rs1061170
CFH
0.060 GeneticVariation BEFREE We also evaluated the association of Y402H with known risk factors for CHD by pooling results from new and in silico studies providing relevant data. 20708732

2010
dbSNP: rs1061170
rs1061170
CFH
0.060 GeneticVariation BEFREE Complement factor H Y402H polymorphism, plasma concentration and risk of coronary artery disease. 18604638

2009
dbSNP: rs1061170
rs1061170
CFH
0.060 GeneticVariation BEFREE We evaluated the association of the Y402H polymorphism with incident coronary heart disease (CHD), incident ischemic stroke, and carotid artery wall thickness (intima-media thickness (IMT)) in the Atherosclerosis Risk in Communities (ARIC) cohort. 18292760

2008
dbSNP: rs1061170
rs1061170
CFH
0.060 GeneticVariation BEFREE CFH Y402H was inversely associated with CHD among women, but not men. 17483111

2007
dbSNP: rs1061170
rs1061170
CFH
0.060 GeneticVariation BEFREE A total of 5,520 participants without history of coronary heart disease was genotyped for the Tyr402His polymorphism of the CFH gene. 16630992

2006