List of variants in gene combination UGT1A, UGT1A1, UGT1A10, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9 reported as likely 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: 10

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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.182C>G (p.Ala61Gly)	rs1273237448	0.00001
NM_000463.3(UGT1A1):c.923G>A (p.Gly308Glu)	rs62625011	0.00001
NM_000463.3(UGT1A1):c.1070A>G (p.Gln357Arg)	rs72551351
NM_000463.3(UGT1A1):c.247T>C (p.Phe83Leu)
NM_000463.3(UGT1A1):c.2_17del (p.Met1fs)	rs2125981899
NM_000463.3(UGT1A1):c.353dup (p.Asp119fs)	rs748219743
NM_000463.3(UGT1A1):c.530G>A (p.Cys177Tyr)	rs1373930486
NM_000463.3(UGT1A1):c.917C>T (p.Ser306Phe)	rs1169717734

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