Variants with conflicting interpretations "likely benign" from ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories and "uncertain significance" from Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease,Montreal Heart Institute

Minimum review status of the submission from ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories:		Collection method of the submission from ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories:
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
NM_001943.5(DSG2):c.166G>A (p.Val56Met)	rs121913013
NM_032578.4(MYPN):c.3335C>T (p.Pro1112Leu)	rs71534278

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