Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
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0.090 | GeneticVariation | BEFREE | As their main finding, they concluded that 'K469E polymorphism is associated with CHD risk and the K allele is a more significant risk factor for developing CHD amongst Chinese and Caucasians populations'. | 31072912 | 2019 |
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0.090 | GeneticVariation | BEFREE | The pooled result showed that the <i>ICAM-1</i> gene E469K</span> polymorphism was significantly associated with an increased risk of CHD (OR = 1.20, 95% CI = 1.11-1.29, for the allele K versus allele E; OR = 1.66, 95% CI = 1.43-1.92, for the K allele carriers versus EE). | 30674642 | 2019 |
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0.090 | GeneticVariation | BEFREE | ICAM-1 gene rs5498 polymorphism decreases the risk of coronary artery disease. | 30290609 | 2018 |
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0.090 | GeneticVariation | BEFREE | Intercellular adhesion molecule-1 K469E polymorphism and risk of coronary artery disease: a meta-analysis. | 25503951 | 2014 |
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0.090 | GeneticVariation | BEFREE | The ICAM-1 K469E polymorphism is associated with the risk of coronary artery disease: a meta-analysis. | 25025994 | 2014 |
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0.090 | GeneticVariation | BEFREE | In conclusion, it was demonstrated in the present study that the rs5498 polymorphism of the ICAM‑1 gene was associated with CHD in males. | 24993975 | 2014 |
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0.090 | GeneticVariation | BEFREE | Intercellular adhesion molecule-1 E469K gene polymorphism and coronary artery disease in the Chinese population: a meta-analysis involving 3065 subjects. | 21987404 | 2012 |
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|
0.090 | GeneticVariation | BEFREE | The pooled result showed that the ICAM1 gene-E469K</span> polymorphism was significantly associated with an increased risk of CHD (OR = 1.496, 95% CI = 1.363-1.642, for the allele K vs. allele E; OR = 1.919, 95% CI = 11.635-2.253, for the K allele carriers vs. EE). | 22203486 | 2012 |
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0.090 | GeneticVariation | BEFREE | Interactions between rs5498 polymorphism in the ICAM1 gene and traditional risk factors influence susceptibility to coronary artery disease. | 19048183 | 2009 |