RS7678555 Unknown gene
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GWAS Studies (15)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| Coronary artery disease | A | OR: 0.96 | 3E-16 | PubMed |
| Aortic valve area (MTAG) | A | β: 0.044 | 3E-16 | PubMed |
| Coronary artery disease | A | β: 0.056 | 3E-15 | PubMed |
| Coronary artery disease | A | β: 0.049 | 1E-14 | PubMed |
| Coronary artery disease or fibrinogen levels (pleiotropy) | — | — | 1E-11 | PubMed |
| Coronary artery disease or factor VII levels (pleiotropy) | — | — | 2E-11 | PubMed |
| Coronary artery disease or factor VIII levels (pleiotropy) | — | — | 2E-11 | PubMed |
| Coronary artery disease or von Willebrand factor levels (pleiotropy) | — | — | 2E-11 | PubMed |
| Coronary artery disease or factor XI levels (pleiotropy) | — | — | 2E-11 | PubMed |
| Aortic valve area | A | β: 0.042 | 2E-11 | PubMed |
| Coronary artery disease (MTAG) | C | OR: 6.28 | 3E-10 | PubMed |
| Coronary artery disease (myocardial infarction, percutaneous transluminal coronary angioplasty, coronary artery bypass grafting, angina or chromic ischemic heart disease) | C | OR: 1.05 | 1E-8 | PubMed |
| Coronary artery disease | C | OR: 1.06 | 3E-8 | PubMed |
| Myocardial infarction | C | OR: 1.04 | 2E-7 | PubMed |
| Myocardial infarction | — | OR: 0.96 | 2E-7 | PubMed |