NM_000506.4:c.*97G>A

Subject ID	Country of Origin	Allele Count	Allele Frequency	CTGA Clinical Significance	Condition(s)	Reference	Remarks
188050.2	Lebanon	1		Pathogenic	Thrombophilia due to thrombin defect	Hoteit et al. 2012
188050.3	Lebanon	1		Pathogenic	Thrombophilia due to thrombin defect	Hoteit et al. 2012
188050.4.1	Lebanon	1		Pathogenic	Thrombophilia due to thrombin defect	Kreidy et al. 2009	25 patients identified with inherited ge...
600880.1	Lebanon	1	NA	Pathogenic	Budd-Chiari Syndrome	Musallam et al, 2010	Patient later developed essential thromb...
601367.1	Lebanon	1		Pathogenic	Stroke, Ischemic	Hoteit et al. 2012
601367.2	Lebanon	1		Pathogenic	Stroke, Ischemic	Hoteit et al. 2012
601367.3	Lebanon	1		Uncertain Significance	Stroke, Ischemic	Araji et al. 2014	Stroke patient with spinal lesion
601367.28	Lebanon	1		Uncertain Significance	Stroke, Ischemic	Araji et al. 2014	Stroke patient with small vessel lesion
601367.31	Lebanon	2		Uncertain Significance	Stroke, Ischemic	Araji et al. 2014	Stroke patient with small vessel lesion
601367.32	Lebanon	1		Uncertain Significance	Stroke, Ischemic	Araji et al. 2014	Stroke patient with small vessel lesion

Epidemiology in the Arab World