Variants with conflicting interpretations "pathogenic" from Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden and "risk factor" from any submitter

Minimum review status of the submission from Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden:		Collection method of the submission from Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden:
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: 2

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HGVS	dbSNP	gnomAD frequency
NM_002485.5(NBN):c.657_661del (p.Lys219fs)	rs587776650
NM_007294.4(BRCA1):c.5266dup (p.Gln1756fs)	rs80357906

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