Unknown
| Variant Name | Allele Count | Allele Frequency | Associated Disease | Associated Gene |
|---|---|---|---|---|
| NM_005957.4:c.665C>T | NA | |||
| NM_005957.4:c.1286A>C | ||||
| NM_000130.4:c.1601G>A | ||||
| NM_000130.4:c.3980A>G |
| Subject Id | Country | HPO Terms | Sex | Family History | Parental Consanguinity | Remarks |
|---|---|---|---|---|---|---|
| 188055.G.2.1 | Lebanon | Deep venous thrombosis | Unknown | Group of 5 patients | ||
| 188055.G.2.2 | Lebanon | Deep venous thrombosis | Unknown | Group of 32 patients | ||
| 188055.G.2.3 | Lebanon | Deep venous thrombosis | Unknown | Group of 4 patients with Factor V Leiden characterised by Prothrombin c.*97G>A (G20210A) mutation |