Variants with conflicting interpretations "benign" from ClinGen Cardiomyopathy Variant Curation Expert Panel and "likely benign" from any submitter

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.2945T>C (p.Met982Thr)	rs145532615	0.00095
NM_000257.4(MYH7):c.930T>C (p.Tyr310=)	rs111626355	0.00091
NM_000257.4(MYH7):c.3156G>A (p.Lys1052=)	rs138294643	0.00063
NM_000257.4(MYH7):c.1322C>T (p.Thr441Met)	rs121913653	0.00006
NM_000257.4(MYH7):c.5736C>T (p.Ile1912=)	rs200728597	0.00002
NM_000257.4(MYH7):c.3770A>G (p.Asn1257Ser)	rs574005462

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