Variants with conflicting interpretations "uncertain significance" from Lab. Molecular Oncology, VUB, Free University of Brussels and "likely benign" from Women's Health and Genetics/Laboratory Corporation of America, LabCorp

Minimum review status of the submission from Lab. Molecular Oncology, VUB, Free University of Brussels:		Collection method of the submission from Lab. Molecular Oncology, VUB, Free University of Brussels:
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: 1

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HGVS	dbSNP	gnomAD frequency
NM_000465.4(BARD1):c.1347A>G (p.Gln449=)	rs373257776	0.00021

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