List of variants in gene combination UGT1A, UGT1A1, UGT1A10, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9 reported as pathogenic for Gilbert syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_001072.4(UGT1A6):c.862-10021T>G	rs4124874	0.56024
UGT1A1*6	rs4148323	0.00891
NM_000463.3(UGT1A1):c.1091C>T (p.Pro364Leu)	rs34946978	0.00053
NM_000463.3(UGT1A1):c.1456T>G (p.Tyr486Asp)	rs34993780	0.00016
NM_000463.3(UGT1A1):c.1021C>T (p.Arg341Ter)	rs72551349	0.00002
NM_000463.2(UGT1A1):c.-53_-52insTA	rs1559406508
NM_000463.3(UGT1A1):c.1270G>T (p.Glu424Ter)	rs2126038122
NM_000463.3(UGT1A1):c.1304+1G>T	rs2126038220
NM_000463.3(UGT1A1):c.492_493del (p.Leu166fs)	rs2125987779
NM_000463.3(UGT1A1):c.686C>A (p.Pro229Gln)	rs35350960
UGT1A1*28	rs3064744

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