List of variants in gene combination UGT1A, UGT1A1, UGT1A10, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9 reported as benign for 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000463.3(UGT1A1):c.864+2925T>G	rs4148324	0.36251
NM_000463.3(UGT1A1):c.864+2842G>T	rs6742078	0.35807
NM_000463.3(UGT1A1):c.996+15T>C	rs4148327	0.00099

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