188055.G.3.3

Lebanon

Hypercoagulability

Variant Name	Allele Count	Associated Disease
NM_000130.4:c.1601G>A	1	Thrombophilia due to Activated Protein C Resistance
NM_000506.4:c.*97G>A	1	Thrombophilia due to thrombin defect Thrombophilia due to Activated Protein C Resistance

Study with 25 patients identified with inherited genetic predisposing factors. Two patients with multiple mutations.

Related Subjects

Subject Id	Country	HPO Terms	Remarks
188055.G.3.1	Lebanon	Hypercoagulability	Study with 25 patients identified with inherited genetic predisposing factors.
188055.G.3.2	Lebanon	Hypercoagulability	Study with 25 patients identified with inherited genetic predisposing factors. Two patients with multiple mutations.