"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "SLC2A2"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 344159	NM_000340.2(SLC2A2):c.1432C>G (p.Leu478Val)	SLC2A2 (L478V +2 more)	Single nucleotide variant (missense variant)	Type 2 diabetes mellitus +3 more	GConflicting classifications of pathogenicity
Select item 255899	NM_000340.2(SLC2A2):c.661C>T (p.Leu221=)	SLC2A2	Single nucleotide variant (synonymous variant)	SLC2A2-related condition +3 more	GBenign/Likely benign
Select item 507994	NM_000340.2(SLC2A2):c.588C>T (p.Ile196=)	SLC2A2	Single nucleotide variant (synonymous variant)	Fanconi-Bickel syndrome +2 more	GLikely benign
Select item 2498940	NM_000340.2(SLC2A2):c.548C>T (p.Ala183Val)	SLC2A2 (A10V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 255898	NM_000340.2(SLC2A2):c.301G>A (p.Val101Ile)	SLC2A2 (V101I)	Single nucleotide variant (missense variant +2 more)	Monogenic diabetes +3 more	GBenign/Likely benign
Select item 516406	NM_000340.2(SLC2A2):c.203C>T (p.Pro68Leu)	SLC2A2 (P68L)	Single nucleotide variant (missense variant +2 more)	Monogenic diabetes +3 more	GBenign/Likely benign

ClinVar