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Prothrombin G20210A is a genetic variation associated with increased blood coagulation (thrombophilia). It increases the risk of blood clots including from deep vein thrombosis, and of pulmonary embolism. One copy of the mutation increases the risk of a blood clot from 1 in 1,000 per year to 2.5 in 1,000. Two copies increases the risk to up to 20 in…
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prothrombin risk blood mutation g20210a increased thrombosis increases factor caucasians genetic 000 thrombophilia clots clotting clot venous thromboembolism gene increase
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Prothrombin G20210A | Frequency | 2% (Caucasians) | 1.00 | infobox |
| Prothrombin G20210A | Other names | Prothrombin thrombophilia, factor II mutation, prothrombin mutation, rs1799963, factor II G20210A | 1.00 | infobox |
| Prothrombin G20210A | Symptoms | Blood clots | 1.00 | infobox |
| Prothrombin G20210A | is a | genetic variation associated with increased blood coagulation | 0.90 | text |
| Prothrombin G20210A | has treatment | Patients | 0.60 | section |
| Prothrombin G20210A | has treatment | Continuing | 0.60 | section |
| Prothrombin G20210A | has treatment | The | 0.60 | section |
| Prothrombin G20210A | has treatment | G20210A | 0.60 | section |
| Prothrombin G20210A | has treatment | However | 0.60 | section |
| Prothrombin G20210A | has treatment | Oral | 0.60 | section |
| Prothrombin G20210A | has treatment | This | 0.60 | section |
| Prothrombin G20210A | related to Diagnosis | Diagnosis | 0.60 | section |
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