"UGT1A1-related disorder"[Disease/phenotype] AND "Rady Children's Inst - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 594666	NM_000463.2(UGT1A1):c.-53_-52insTA	UGT1A6, UGT1A9 +8 more	Insertion (intron variant)	UGT1A1-related disorder +1 more	GPathogenic; other
Select item 212545	NM_000463.3(UGT1A1):c.722_723del (p.Glu241fs)	UGT1A5, UGT1A6 +8 more (E241fs)	Microsatellite (frameshift variant +1 more)	UGT1A1-related disorder +2 more	GPathogenic