Variants with conflicting interpretations "likely pathogenic" from Institute of Medical Molecular Genetics, University of Zurich and "likely benign" from any submitter

Minimum review status of the submission from Institute of Medical Molecular Genetics, University of Zurich:		Collection method of the submission from Institute of Medical Molecular Genetics, University of Zurich:
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_201253.3(CRB1):c.498_506del (p.Ile167_Gly169del)	rs398124615

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