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

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) 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: 11

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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.1091C>T (p.Pro364Leu)	rs34946978	0.00053
NM_000463.3(UGT1A1):c.674T>G (p.Val225Gly)	rs35003977	0.00034
NM_000463.3(UGT1A1):c.1456T>G (p.Tyr486Asp)	rs34993780	0.00016
NM_000463.3(UGT1A1):c.524T>A (p.Leu175Gln)	rs72551341	0.00005
NM_000463.3(UGT1A1):c.1381T>C (p.Trp461Arg)	rs1476500325	0.00001
NM_000463.3(UGT1A1):c.923G>A (p.Gly308Glu)	rs62625011	0.00001
NM_000463.3(UGT1A1):c.1084+1G>T	rs587784535
NM_000463.3(UGT1A1):c.80_93del (p.Ala27fs)	rs775463336
UGT1A1*28	rs3064744

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