Variants with conflicting interpretations "benign" from Research Molecular Genetics Laboratory, Women's College Hospital, University of Toronto and "benign" from any submitter

Minimum review status of the submission from Research Molecular Genetics Laboratory, Women's College Hospital, University of Toronto:		Collection method of the submission from Research Molecular Genetics Laboratory, Women's College Hospital, University of Toronto:
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_007294.4(BRCA1):c.1067A>G (p.Gln356Arg)	rs1799950	0.04695
NM_000059.4(BRCA2):c.10234A>G (p.Ile3412Val)	rs1801426	0.03864
NM_000059.4(BRCA2):c.9976A>T (p.Lys3326Ter)	rs11571833	0.00597
NM_007294.4(BRCA1):c.4535G>T (p.Ser1512Ile)	rs1800744	0.00240

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