Variants with conflicting interpretations "likely pathogenic" from Division of Medical Genetics, University of Washington and "uncertain significance" 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: 1

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HGVS	dbSNP	gnomAD frequency
NM_007194.4(CHEK2):c.480AGA[1] (p.Glu161del)	rs587782008

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