Variants with conflicting interpretations "uncertain significance" from Foulkes Cancer Genetics LDI, Lady Davis Institute for Medical Research and "benign" from CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario

Minimum review status of the submission from Foulkes Cancer Genetics LDI, Lady Davis Institute for Medical Research:		Collection method of the submission from Foulkes Cancer Genetics LDI, Lady Davis Institute for Medical Research:
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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.5704G>A	rs4987048	0.00655
NM_000059.4(BRCA2):c.8149G>T (p.Ala2717Ser)	rs28897747	0.00127
NM_000059.4(BRCA2):c.6821G>T (p.Gly2274Val)	rs55712212	0.00126
NM_000059.4(BRCA2):c.6322C>T (p.Arg2108Cys)	rs55794205	0.00019

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