188055.G.3.2

Lebanon

Hypercoagulability

Variant Name	Allele Count	Allele Frequency	Associated Disease	Associated Gene
NM_005957.4:c.665C>T	2		Thrombophilia due to thrombin defect
NM_000130.4:c.1601G>A	2		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	Sex	Family History	Parental Consanguinity	Remarks
188055.G.3.1	Lebanon	Hypercoagulability				Study with 25 patients identified with inherited genetic predisposing factors.
188055.G.3.3	Lebanon	Hypercoagulability				Study with 25 patients identified with inherited genetic predisposing factors. Two patients with multiple mutations.