List of variants in gene combination UGT1A, UGT1A1, UGT1A10, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9 reported as pathogenic by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 8

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HGVS	dbSNP	gnomAD frequency
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.1220del (p.Lys407fs)	rs558109660
NM_000463.3(UGT1A1):c.222C>A (p.Tyr74Ter)	rs72551340
NM_000463.3(UGT1A1):c.686C>A (p.Pro229Gln)	rs35350960
UGT1A1*28	rs3064744
UGT1A1*37	rs3064744

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