Variants with conflicting interpretations "uncertain significance" from Department of Pathology and Molecular Medicine, Queen's University and "benign" from any submitter

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.3708T>G (p.Asn1236Lys)	rs28897687	0.00031
NM_000059.4(BRCA2):c.7448G>A (p.Ser2483Asn)	rs80358967	0.00001
NM_000059.4(BRCA2):c.1909+22del	rs276174816
NM_000059.4(BRCA2):c.68-7del	rs276174878
NM_000059.4(BRCA2):c.6841+80_6841+83del	rs11571661

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