C0007194[trait identifier] AND "Molecular Cardiogenetic Lab, Hospices - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 692113	NM_000256.3(MYBPC3):c.2905+445_2905+448del	MYBPC3	Deletion (intron variant)	Hypertrophic cardiomyopathy	GPathogenic
Select item 692114	NM_000256.3(MYBPC3):c.1927+600C>T	MYBPC3	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy 4 +1 more	GLikely pathogenic
Select item 693982	NM_000256.3(MYBPC3):c.1224-80G>A	MYBPC3	Single nucleotide variant (intron variant)	not provided +1 more	GLikely pathogenic

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