Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
---|---|---|---|---|---|---|---|---|---|---|
|
0.090 | GeneticVariation | BEFREE | Our study aims to explore the association of rs7025486 single-nucleotide polymorphisms (SNP) in DAB2IP and rs1333049 on chromosome 9p21.3 with the coronary artery disease in Chinese population. | 28962556 | 2017 |
||||
|
0.090 | GeneticVariation | BEFREE | Association Study Between Coronary Artery Disease and rs1333049 Polymorphism at 9p21.3 Locus in Italian Population. | 28639227 | 2017 |
||||
|
0.090 | GeneticVariation | BEFREE | The leading coronary artery disease-associated SNP rs1333049 was associated with coronary artery disease; however, none of the 9p21 SNP evaluated in the present study were associated with extreme longevity. | 25257646 | 2015 |
||||
|
0.090 | GeneticVariation | BEFREE | A replication study and a meta-analysis of the association between the CDKN2A rs1333049 polymorphism and coronary heart disease. | 24930384 | 2014 |
||||
|
0.090 | GeneticVariation | BEFREE | Independent association of the variant rs1333049 at the 9p21 locus and coronary heart disease. | 21874923 | 2011 |
||||
|
0.090 | GeneticVariation | BEFREE | Within the chr9p21.3 locus, the single-nucleotide polymorphism rs1333049 has been demonstrated to be most strongly associated with susceptibility to developing coronary artery disease. | 20400779 | 2010 |
||||
|
0.090 | GeneticVariation | BEFREE | Recent genetic studies identified the rs1333049 variant on chromosome 9p21 as a major susceptibility locus for coronary artery disease and myocardial infarction (MI). | 20231156 | 2010 |
||||
|
0.090 | GeneticVariation | BEFREE | We genotyped the rs1333049 single-nucleotide polymorphism in 593 Caucasian individuals with stable coronary artery disease recruited in the Heart and Soul Study. | 19171343 | 2009 |
||||
|
0.090 | GeneticVariation | BEFREE | Of thousands of chromosomal loci studied, the same locus had the strongest association with coronary artery disease in both the WTCCC and the German studies: chromosome 9p21.3 (SNP, rs1333049) (P=1.80x10(-14) and P=3.40x10(-6), respectively). | 17634449 | 2007 |