Variants with conflicting interpretations "pathogenic" from Core Molecular Diagnostic Lab, McGill University Health Centre and "likely pathogenic" from any submitter

Minimum review status of the submission from Core Molecular Diagnostic Lab, McGill University Health Centre:		Collection method of the submission from Core Molecular Diagnostic Lab, McGill University Health Centre:
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_001792.5(CDH2):c.1057G>A (p.Asp353Asn)	rs1599017933
NM_014297.5(ETHE1):c.79C>A (p.Gln27Lys)	rs749803238

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