List of variants in gene combination UGT1A, UGT1A10, UGT1A7, UGT1A8, UGT1A9 reported as benign 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_019076.5(UGT1A8):c.855+63766C>A	rs17863778	0.61291
NM_019076.5(UGT1A8):c.855+63767G>A	rs17868324	0.61271
NM_019076.5(UGT1A8):c.855+63762T>G	rs17868323	0.61254
NM_019076.5(UGT1A8):c.855+63997T>C	rs11692021	0.33934
NM_019076.5(UGT1A8):c.855+63408C>A	rs7577677	0.33834
NM_019076.5(UGT1A8):c.855+64131G>A	rs17864686	0.18037
NM_019076.5(UGT1A8):c.855+63766_855+63767delinsAA	rs386656364

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