"Agnes Ginges Centre for Molecular Cardiology, Centenary Institute"[su - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 848489	NM_000258.3(MYL3):c.466G>C (p.Val156Leu)	MYL3 (V156L)	Single nucleotide variant (missense variant)	Restrictive cardiomyopathy +1 more	GUncertain significance
Select item 31783	NM_000258.3(MYL3):c.463C>G (p.His155Asp)	MYL3 (H155D)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 14062	NM_000258.3(MYL3):c.461G>A (p.Arg154His)	MYL3 (R154H)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +4 more	GUncertain significance
Select item 43124	NM_000258.3(MYL3):c.460C>T (p.Arg154Cys)	MYL3 (R154C)	Single nucleotide variant (missense variant)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 43121	NM_000258.3(MYL3):c.170C>A (p.Ala57Asp)	MYL3 (A57D)	Single nucleotide variant (missense variant)	Long QT syndrome +5 more	GConflicting classifications of pathogenicity
Select item 426762	NM_000258.3(MYL3):c.152T>C (p.Ile51Thr)	MYL3 (I51T)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy +3 more	GUncertain significance

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