Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
0.900 GeneticVariation BEFREE While we confirmed the association of rs10757278 with CDKN2B expression in MI patients, we failed to find an association between the investigated variants and MI or disease burden. 31386834 2019
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
0.900 GeneticVariation BEFREE The aim of the study was to find whether patients carrying polymorphic allele of the rs10757278 polymorphism from 9p21 locus have changed risk of arrhythmia (atrial fibrillation, AF; sustained ventricular tachycardia or ventricular fibrillation, sVT/VF) during acute phase of myocardial infarction. 26615606 2016
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
0.900 GeneticVariation BEFREE We found even more significant association between rs</span>10757278 polymorphism and MI in pooled population, p = 3.55 × 10-53, after excluding the study from the Pakistan population. 26006241 2015
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
0.900 GeneticVariation BEFREE Genome-wide association studies have identified 2 single-nucleotide polymorphisms (SNPs) on chromosome arm 9p21, rs10757278, and rs2383207 that confer susceptibility to myocardial infarction. 23454037 2013
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
0.900 GeneticVariation BEFREE We replicated the association between the rs10757278 SNP and myocardial infarction and binary (presence/absence) angiographic classifications of CAD. 20729229 2010
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
0.900 GeneticVariation BEFREE Background Two single nucleotide polymorphisms (SNPs, rs10757278 and rs2383207) on chromosome 9p21 have been proved to be associated with myocardial infarction. 18459066 2009
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
0.900 GeneticVariation BEFREE We related SNPs rs2383207 and rs10757278 to stroke and to myocardial infarction and coronary revascularizations (coronary events) using crude and multivariate adjusted Cox proportional hazards models. 19293724 2009
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
0.900 GeneticVariation BEFREE A common variant at chromosome 9p21 (tagged by the rs1333049 or rs10757278 single-nucleotide polymorphism) is strongly associated with myocardial infarction and major arterial aneurysms. 20031606 2009
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
0.900 GeneticVariation BEFREE This study presents the first analysis of these SNPs (rs10757274, rs2383206, rs2383207, and rs10757278) in a premature, familial CAD/MI population (GeneQuest). 18505420 2008
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
0.900 GeneticVariation BEFREE Genome-wide single nucleotide polymorphism (SNP) association studies recently identified four SNPs (rs10757274, rs2383206, rs2383207, and rs10757278) on chromosome 9p21 that were associated with coronary artery disease (CAD) and myocardial infarction (MI) in Caucasian populations from northern Europe and North America. 18066490 2008
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
0.900 GeneticVariation BEFREE Recent genome-wide association studies have identified 4 SNPs on chromosome 9p21 associated with CAD (rs10757274 and rs2383206) and myocardial infarction (MI: rs2383207 and rs10757278) in White populations in Northern Europe and North America. 18048766 2008
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
0.900 GeneticVariation BEFREE Recent genome wide association (GWA) studies identified two Single Nucleotide Polymorphisms (SNP) (rs10757278 and rs10757274) in the region of the CDK2NA and CDK2NB genes to be consistently associated with the risks of coronary heart disease (CHD) and myocardial infarction (MI). 18925945 2008
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
0.900 GeneticVariation GWASCAT A common variant on chromosome 9p21 affects the risk of myocardial infarction. 17478679 2007
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
0.900 GeneticVariation GWASDB A common variant on chromosome 9p21 affects the risk of myocardial infarction. 17478679 2007