Variants with conflicting interpretations "likely benign" from Department of Medical Genetics, University Hospital of North Norway and "benign" from any submitter

Minimum review status of the submission from Department of Medical Genetics, University Hospital of North Norway:		Collection method of the submission from Department of Medical Genetics, University Hospital of North Norway:
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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.68-7T>A	rs81002830	0.00277
NM_000059.4(BRCA2):c.6100C>T (p.Arg2034Cys)	rs1799954	0.00268
NM_007294.4(BRCA1):c.2521C>T (p.Arg841Trp)	rs1800709	0.00137
NM_000059.4(BRCA2):c.6821G>T (p.Gly2274Val)	rs55712212	0.00126
NM_007294.4(BRCA1):c.1487G>A (p.Arg496His)	rs28897677	0.00060
NM_007294.4(BRCA1):c.548-17G>T	rs80358014	0.00028
NM_000059.4(BRCA2):c.2680G>A (p.Val894Ile)	rs28897715	0.00011
NM_000059.4(BRCA2):c.3568C>T (p.Arg1190Trp)	rs80358604	0.00007
NM_000059.4(BRCA2):c.750G>A (p.Val250=)	rs143214959	0.00005
NM_007294.4(BRCA1):c.5117G>C (p.Gly1706Ala)	rs80356860	0.00005

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