Unknown
| Variant Name | Allele Count | Allele Frequency | Associated Disease | Associated Gene |
|---|---|---|---|---|
| NM_000130.4:c.1601G>A | 1 | NA |
| 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.2.3 | Lebanon | Deep venous thrombosis | Unknown | Group of 4 patients with Factor V Leiden characterised by Prothrombin c.*97G>A (G20210A) mutation | ||
| 188055.G.2.4 | Lebanon | Deep venous thrombosis | Unknown | 14 patients with Factor V Leiden characterised by MTHFR c.665C>T (C677T), MTHFR c.1286A>C, or Factor V c.3980A>G (H1299R) mutation |