Variants with conflicting interpretations "uncertain significance" from ClinGen Cardiomyopathy Variant Curation Expert Panel and "likely pathogenic" from Labcorp Genetics (formerly Invitae), Labcorp

Minimum review status of the submission from ClinGen Cardiomyopathy Variant Curation Expert Panel:		Collection method of the submission from ClinGen Cardiomyopathy Variant Curation Expert Panel:
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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.1193G>A (p.Gly398Glu)	rs730880158	0.00002
NM_000257.4(MYH7):c.5422G>A (p.Gly1808Ser)	rs369940645	0.00002
NM_000257.4(MYH7):c.2804A>T (p.Glu935Val)	rs730880761	0.00001
NM_000257.4(MYH7):c.3337G>A (p.Ala1113Thr)	rs193922388	0.00001
NM_000257.4(MYH7):c.610C>T (p.Arg204Cys)	rs397516259	0.00001
NM_000257.4(MYH7):c.2714G>C (p.Cys905Ser)	rs730880757

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