Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs854560
rs854560
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation BEFREE Relationship between rs854560 <i>PON1</i> Gene Polymorphism and Tobacco Smoking with Coronary Artery Disease. 29118461

2017

dbSNP: rs854560
rs854560
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation BEFREE The association of paraoxonase 1 gene L55M polymorphism with the extent and severity of coronary artery disease in the Turkish population and its dependence on gender. 26467378

2016

dbSNP: rs854560
rs854560
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation BEFREE The activity of PON1 is decreased in patients with coronary artery disease, myocardial infarction or chronic kidney disease. rs662 and rs854560 are single nucleotide polymorphisms (SNPs) associated with PON1 activity and 10-year cardiovascular mortality of patients with stable coronary artery disease. 25155309

2016

dbSNP: rs854560
rs854560
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation BEFREE A preliminary study of human paraoxonase and PON 1 L/M55-PON 1 Q/R 192 polymorphisms in Turkish patients with coronary artery disease. 19226538

2009

dbSNP: rs854560
rs854560
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation BEFREE In parallel nested case-control studies, the prospective associations between PON1 polymorphisms Q192R and L55M and incident CHD were examined among participants in the Nurses' Health and Health Professionals Follow-up Studies. 19443958

2009

dbSNP: rs854560
rs854560
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation BEFREE In contrast to previous suggestions, this meta-analysis shows no significant association of CHD with the L55M or T(-107)C polymorphism in PON1 or with the S311C polymorphism in PON2. 15001326

2004

dbSNP: rs854560
rs854560
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation BEFREE Two coding polymorphisms, 55M/L and 192Q/R, and a promoter variant, -107C/T, has been extensively studied with respect to susceptibility to CHD. 15241482

2004

dbSNP: rs854560
rs854560
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation BEFREE PON1 M/L55 mutation protects high-risk patients against coronary artery disease. 14996478

2004

dbSNP: rs854560
rs854560
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation BEFREE Genotype frequencies did not differ between cases and controls but the CHD risk associated with smoking was significantly modified by PON1 L55M genotype. 14636952

2003

dbSNP: rs854560
rs854560
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation BEFREE The L55M-glucose interaction differentiated offspring of high CHD risk families, suggesting that it may be of particular relevance for vascular disease and possibly other diabetic complications. 11889198

2002

dbSNP: rs854560
rs854560
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation BEFREE The objective of this study was to determine the possible relationship between the two human PON1 amino acid variants, the Leu55Met and the Gln192Arg polymorphism, and the risk of CHD in a community-dwelling cohort of European ancestry. 12417809

2002