Table 1.

Mutations found in monogenic diabetes causative genes

	Gene	Variant	Clinical Significance
Patient 1	INS	c0.152 C > G	MODY10
Patient 2	HNF1A	c0.527-6_527-3delCTGC	MODY3
Patients 3, 4	HNF1A	c0.955 + 1G > A	MODY3
Patient 5	WFS1	c0.2643_2646delCTTT	Wolfram syndrome
Patient 6	WFS1	c0.1433G > A,	Wolfram syndrome
Patient 7	SLC29A3	c0.1228C > T	H syndrome
Patient 8	KLF11	c0.1298A > G	Variant of uncertain significance
Patient 9	KLF11	c0.1298 A > G	Variant of uncertain significance
Patient 10	PDX1	c0.98C > A	Variant of uncertain significance