"Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Child - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 218787	NM_021027.3(UGT1A9):c.855+45828G>A	UGT1A, UGT1A10 +5 more	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 218786	NM_021027.3(UGT1A9):c.1420G>T (p.Ala474Ser)	UGT1A4, UGT1A9 +8 more (A474S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance