MMRN1, multimerin 1, 22915

N. diseases: 272; N. variants: 3
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.070 GeneticVariation disease BEFREE This study was aimed to investigate the clinical relevance between glycoprotein Ia (GPIA) rs1126643C/T polymorphism and the outcome of coronary artery disease after coronary artery bypass graft (CABG) surgery and explore the involved potential mechanisms. 27881421 2016
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.070 GeneticVariation disease BEFREE Lack of association between the platelet glycoprotein Ia C807T gene polymorphism and coronary artery disease: a meta-analysis. 17023078 2007
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.070 GeneticVariation disease BEFREE Our results may question the potential role of C807T the GPIa anomaly as a single genetic abnormality predisposing young men to coronary artery disease. 16136407 2005
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.070 GeneticVariation disease BEFREE Variability in platelet aggregation following sustained aspirin and clopidogrel treatment in patients with coronary heart disease and influence of the 807 C/T polymorphism of the glycoprotein Ia gene. 16214444 2005
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.070 GeneticVariation disease BEFREE Association of the gene polymorphisms of platelet glycoprotein Ia and IIb/IIIa with myocardial infarction and extent of coronary artery disease in the Korean population. 15227729 2004
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.070 Biomarker disease BEFREE Platelet glycoprotein Ia gene dimorphism alpha2-807 in malignant arrhythmia in coronary artery disease. 10822074 2000
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.070 GeneticVariation disease BEFREE The impact of the glycoprotein Ia collagen receptor subunit A1648G gene polymorphism on coronary artery disease and acute myocardial infarction. 10744142 2000