| Variant Name | Allele Count | Allele Frequency | Associated Disease | Associated Gene |
|---|---|---|---|---|
| NM_000130.4:c.1601G>A | 12 |
| Subject Id | Country | HPO Terms | Sex | Family History | Parental Consanguinity | Remarks |
|---|---|---|---|---|---|---|
| 188055.G.3.2 | Lebanon | Hypercoagulability | Study with 25 patients identified with inherited genetic predisposing factors. Two patients with multiple mutations. | |||
| 188055.G.3.3 | Lebanon | Hypercoagulability | Study with 25 patients identified with inherited genetic predisposing factors. Two patients with multiple mutations. |