NM_004646.3:c.1317T>G

Subject ID	Country of Origin	Allele Count	CTGA Clinical Significance	Condition(s)	Reference	Remarks
256300.1.1	Lebanon	2	Pathogenic	Nephrotic Syndrome, Type 1	Gharibeh et al, 2015	While the homozygous mutation led to con...
256300.1.2	Lebanon	2	Pathogenic	Nephrotic Syndrome, Type 1	Gharibeh et al, 2015	Sister of 256300.1.1
256300.1.3	Lebanon	2	Pathogenic	Nephrotic Syndrome, Type 1	Gharibeh et al, 2015	Brother of 256300.1.1
256300.1.4	Lebanon	2	Pathogenic	Nephrotic Syndrome, Type 1	Gharibeh et al, 2015	Brother of 256300.1.1
256300.1.5	Lebanon	1	Pathogenic		Gharibeh et al, 2015	Brother of 256300.1.1
256300.1.6	Lebanon	1	Pathogenic		Gharibeh et al, 2015	Father of 256300.1.1
256300.1.7	Lebanon	1	Pathogenic		Gharibeh et al, 2015	Mother of 256300.1.1

Epidemiology in the Arab World