"Personalized Diabetes Medicine Program, University of Maryland School - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 549537	NM_178161.3(PTF1A):c.265C>A (p.Leu89Ile)	PTF1A (L89I)	Single nucleotide variant (missense variant)	Inborn genetic diseases +3 more	GUncertain significance
Select item 130054	NM_178161.3(PTF1A):c.269G>C (p.Gly90Ala)	PTF1A (G90A)	Single nucleotide variant (missense variant)	Monogenic diabetes +4 more	GConflicting classifications of pathogenicity
Select item 917466	NM_178161.3(PTF1A):c.283G>C (p.Gly95Arg)	PTF1A (G95R)	Single nucleotide variant (missense variant)	Monogenic diabetes	GUncertain significance
Select item 917467	NM_178161.3(PTF1A):c.343C>T (p.Pro115Ser)	PTF1A (P115S)	Single nucleotide variant (missense variant)	Monogenic diabetes	GUncertain significance
Select item 917468	NM_178161.3(PTF1A):c.440C>T (p.Ala147Val)	PTF1A (A147V)	Single nucleotide variant (missense variant)	Monogenic diabetes	GUncertain significance
Select item 917469	NM_178161.3(PTF1A):c.520C>T (p.Arg174Trp)	PTF1A (R174W)	Single nucleotide variant (missense variant)	Monogenic diabetes	GUncertain significance
Select item 299627	NM_178161.3(PTF1A):c.960C>A (p.Asn320Lys)	PTF1A (N320K)	Single nucleotide variant (missense variant)	Monogenic diabetes +1 more	GUncertain significance

ClinVar