Variants with conflicting interpretations "likely pathogenic" from Division of Medical Genetics, University of Washington and "pathogenic" from any submitter

Minimum review status of the submission from Division of Medical Genetics, University of Washington:		Collection method of the submission from Division of Medical Genetics, University of Washington:
Minimum review status of the other submission:		Collection method of the other submission:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 3

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HGVS	dbSNP	gnomAD frequency
NM_058216.3(RAD51C):c.774del (p.Thr259fs)	rs754367349	0.00004
NM_000368.5(TSC1):c.2818C>T (p.Gln940Ter)	rs1588290078
NM_001943.5(DSG2):c.1319_1320del (p.Val440fs)	rs775256998

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