"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "SLC2A2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 130348	NM_000340.2(SLC2A2):c.1437C>T (p.Phe479=)	SLC2A2	Single nucleotide variant (synonymous variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 255900	NM_000340.2(SLC2A2):c.776-15C>T	SLC2A2	Single nucleotide variant (intron variant)	Fanconi-Bickel syndrome +3 more	GBenign
Select item 1693879	NM_000340.2(SLC2A2):c.683G>A (p.Arg228Gln)	SLC2A2 (R109Q +2 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 130351	NM_000340.2(SLC2A2):c.594G>A (p.Thr198=)	SLC2A2	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign
Select item 130350	NM_000340.2(SLC2A2):c.496+8A>T	SLC2A2	Single nucleotide variant (intron variant)	not provided +2 more	GBenign
Select item 130349	NM_000340.2(SLC2A2):c.329C>T (p.Thr110Ile)	SLC2A2 (T110I)	Single nucleotide variant (missense variant +2 more)	not specified +2 more	GBenign
Select item 426982	NM_000340.2(SLC2A2):c.158G>A (p.Arg53Gln)	SLC2A2 (R53Q)	Single nucleotide variant (missense variant +2 more)	Type 2 diabetes mellitus +2 more	GConflicting classifications of pathogenicity

ClinVar