188050.G.2.2

Lebanon

Deep venous thrombosis

Unknown

Variant Name	Allele Count	Allele Frequency	Associated Disease
NM_005957.4:c.665C>T	8		Thrombophilia due to thrombin defect
NM_000130.4:c.1601G>A	4	NA	Thrombophilia due to thrombin defect
NM_000506.4:c.*97G>A	4		Thrombophilia due to thrombin defect

4 patients

Related Subjects

Subject Id	Country	HPO Terms	Sex	Remarks
188050.G.2.1	Lebanon	Deep venous thrombosis	Unknown	10 patients