Unknown
Variant Name | Allele Count | Allele Frequency | Associated Disease | Associated Gene |
---|---|---|---|---|
NM_000130.4:c.1601G>A | ||||
NM_000506.4:c.*97G>A |
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.2.4 | 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 |