Variants with conflicting interpretations "uncertain significance" from Centre of Medical Genetics, University of Antwerp and "pathogenic" from any submitter

Minimum review status of the submission from Centre of Medical Genetics, University of Antwerp:		Collection method of the submission from Centre of Medical Genetics, University of Antwerp:
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_001711.6(BGN):c.908A>C (p.Gln303Pro)	rs886037824

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