"Revvity Omics, Revvity"[submitter] AND "SLC2A9"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2069944	NM_020041.3(SLC2A9):c.1369G>A (p.Val457Ile)	SLC2A9 (V428I +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1928845	NM_020041.3(SLC2A9):c.1339C>T (p.Arg447Trp)	SLC2A9 (R447W +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 4596	NM_020041.3(SLC2A9):c.1138C>T (p.Arg380Trp)	SLC2A9 (R380W +1 more)	Single nucleotide variant (missense variant)	Hypouricemia, renal, 2 +1 more	GConflicting classifications of pathogenicity
Select item 2436015	NM_020041.3(SLC2A9):c.1105G>A (p.Val369Ile)	SLC2A9 (V340I +1 more)	Single nucleotide variant (missense variant)	Hypouricemia, renal, 2	GUncertain significance
Select item 2436013	NM_020041.3(SLC2A9):c.94G>A (p.Ala32Thr)	SLC2A9 (A32T)	Single nucleotide variant (missense variant +1 more)	Hypouricemia, renal, 2	GUncertain significance
Select item 2436014	NM_020041.3(SLC2A9):c.62C>T (p.Thr21Ile)	SLC2A9 (T21I)	Single nucleotide variant (missense variant +1 more)	Hypouricemia, renal, 2	GUncertain significance

ClinVar