List of variants in gene combination UGT1A, UGT1A10, UGT1A7, UGT1A8, UGT1A9 reported as uncertain significance 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_019077.3(UGT1A7):c.352G>T (p.Asp118Tyr)	rs140814031	0.00252
NM_019076.5(UGT1A8):c.855+64203C>A	rs141393523	0.00172
NM_019075.4(UGT1A10):c.855+44822C>T	rs151080578	0.00040
NM_019075.4(UGT1A10):c.855+44982G>C	rs72551332	0.00029
NM_019075.4(UGT1A10):c.855+45231T>C	rs773325642	0.00006
NM_019075.4(UGT1A10):c.855+44683G>A	rs373408916	0.00004
NM_019075.4(UGT1A10):c.855+45414T>C	rs147013594	0.00004
NM_019077.3(UGT1A7):c.565T>C (p.Tyr189His)	rs773379672	0.00001
NM_019075.4(UGT1A10):c.855+44828T>C	rs1575428418
NM_019076.5(UGT1A8):c.855+63716A>G
NM_019076.5(UGT1A8):c.855+64228A>G

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