List of variants in gene combination UGT1A, UGT1A1, UGT1A10, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9 reported as uncertain significance for Bilirubin, serum level of, quantitative trait locus 1; Crigler-Najjar syndrome type 1; Lucey-Driscoll syndrome; Crigler-Najjar syndrome, type II; Gilbert syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
UGT1A1*6	rs4148323	0.00891
NM_000463.3(UGT1A1):c.1352C>T (p.Pro451Leu)	rs114982090	0.00018
NM_000463.3(UGT1A1):c.1324C>T (p.Arg442Cys)	rs143033456	0.00009
NM_000463.3(UGT1A1):c.1099C>T (p.Arg367Cys)	rs55750087	0.00003
NM_000463.3(UGT1A1):c.1207C>T (p.Arg403Cys)	rs778766461	0.00003
NM_000463.3(UGT1A1):c.137C>T (p.Ala46Val)	rs886044683	0.00001
NM_000463.3(UGT1A1):c.1198A>C (p.Asn400His)	rs28934877
NM_000463.3(UGT1A1):c.1387G>A (p.Glu463Lys)
NM_000463.3(UGT1A1):c.449C>G (p.Thr150Arg)
NM_000463.3(UGT1A1):c.536T>A (p.Leu179Gln)
NM_000463.3(UGT1A1):c.686C>A (p.Pro229Gln)	rs35350960
NM_000463.3(UGT1A1):c.686C>T (p.Pro229Leu)	rs35350960
UGT1A1*28	rs3064744

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