Variants in gene combination UGT1A, UGT1A1, UGT1A10, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9 with conflicting interpretations reported as "likely benign and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 12

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HGVS	dbSNP	gnomAD frequency
UGT1A1*6	rs4148323	0.00891
NM_000463.3(UGT1A1):c.540A>G (p.Glu180=)	rs148755655	0.00201
NM_000463.3(UGT1A1):c.1122T>C (p.Gly374=)	rs139698110	0.00126
NM_000463.3(UGT1A1):c.326T>C (p.Val109Ala)	rs144217005	0.00098
NM_000463.3(UGT1A1):c.159G>A (p.Arg53=)	rs149071335	0.00036
NM_000463.3(UGT1A1):c.1352C>T (p.Pro451Leu)	rs114982090	0.00018
NM_000463.3(UGT1A1):c.1026A>T (p.Pro342=)	rs747062491	0.00013
NM_000463.3(UGT1A1):c.189C>T (p.Asp63=)	rs191471887	0.00009
NM_000463.3(UGT1A1):c.1231G>T (p.Val411Leu)	rs36076514	0.00006
NM_000463.3(UGT1A1):c.1458C>T (p.Tyr486=)	rs142077822	0.00005
NM_000463.3(UGT1A1):c.477C>T (p.Ile159=)	rs199766420	0.00005
NM_000463.3(UGT1A1):c.1161C>T (p.Pro387=)	rs763217521	0.00001

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