"Center for Genomic Medicine, King Faisal Specialist Hospital and Rese - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 160239	NM_000463.3(UGT1A1):c.674T>G (p.Val225Gly)	UGT1A, UGT1A1 +8 more (V225G)	Single nucleotide variant (missense variant +1 more)	Hyperbilirubinemia +6 more	GConflicting classifications of pathogenicity; other
Select item 12283	NM_000463.3(UGT1A1):c.1070A>G (p.Gln357Arg)	UGT1A, UGT1A1 +8 more (Q357R +4 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely pathogenic