List of variants in gene combination UGT1A, UGT1A1, UGT1A10, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000463.3(UGT1A1):c.540A>G (p.Glu180=)	rs148755655	0.00201
NM_000463.3(UGT1A1):c.141C>T (p.Ile47=)	rs34526305	0.00154
NM_000463.3(UGT1A1):c.1122T>C (p.Gly374=)	rs139698110	0.00126
NM_000463.3(UGT1A1):c.294T>C (p.Asn98=)	rs138183896	0.00011

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