Variants with conflicting interpretations "uncertain significance" from Department of Pathology and Molecular Medicine, Queen's University and "benign" from Clinical Genetics Laboratory, Department of Pathology, Netherlands Cancer Institute

Minimum review status of the submission from Department of Pathology and Molecular Medicine, Queen's University:		Collection method of the submission from Department of Pathology and Molecular Medicine, Queen's University:
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_000059.4(BRCA2):c.6841+80_6841+83del	rs11571661

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