 | | VARIANT: 2147v2 | |
| Entry |
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| Name |
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| Type |
Loss of function
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| Gene |
F2 coagulation factor II, thrombin [KO: K01313]
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| Organism |
hsa_var Human gene variants (Homo sapiens)
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| Variation |
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| Network |
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| Disease |
| H00223 | Inherited thrombophilia |
| H01254 | Congenital prothrombin deficiency |
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| Reference |
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| Authors |
Dautaj A, Krasi G, Bushati V, Precone V, Gheza M, Fioretti F, Sartori M, Costantini A, Benedetti S, Bertelli M |
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| Title |
Hereditary thrombophilia. |
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| Journal |
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| Reference |
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| Authors |
Zhang Y, Zhang Z, Shu S, Niu W, Xie W, Wan J, Zhai Z, Wang C |
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| Title |
The genetics of venous thromboembolism: a systematic review of thrombophilia families. |
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| Journal |
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| LinkDB |
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