"Centogene AG - the Rare Disease Company"[submitter] AND "MYH7"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 42096	NM_000257.4(MYH7):c.5177AGA[3] (p.Lys1729del)	LOC126861897, MHRT +1 more (K1729del)	Microsatellite (inframe_deletion +1 more)	MYH7-related skeletal myopathy +2 more	GPathogenic
Select item 14095	NM_000257.4(MYH7):c.2167C>T (p.Arg723Cys)	MYH7 (R723C)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy	GPathogenic FDA Recognized database