188050.4.1

Lebanon

Hypercoagulability

Variant Name	Allele Count	Associated Disease
NM_000506.4:c.*97G>A	1	Thrombophilia due to thrombin defect

25 patients identified with inherited genetic predisposing factors.

Related Subjects

Subject Id	Country	HPO Terms	Remarks
188050.4.G.1	Lebanon	Hypercoagulability	Study with 25 patients identified with inherited genetic predisposing factors.