"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC126861 - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 177763	NM_000257.4(MYH7):c.2678C>T (p.Ala893Val)	LOC126861898, MYH7 (A893V)	Single nucleotide variant (missense variant)	Primary dilated cardiomyopathy	GUncertain significance FDA Recognized database
Select item 2630460	NM_000257.4(MYH7):c.2554A>G (p.Met852Val)	LOC126861898, MYH7 (M852V)	Single nucleotide variant (missense variant)	MYH7-related disorder	GUncertain significance
Select item 42915	NM_000257.4(MYH7):c.2553C>A (p.Ser851=)	LOC126861898, MYH7	Single nucleotide variant (synonymous variant)	Cardiomyopathy	GBenign FDA Recognized database
Select item 42907	NM_000257.4(MYH7):c.2472C>T (p.Val824=)	LOC126861898, MYH7	Single nucleotide variant (synonymous variant)	Cardiomyopathy +5 more	GConflicting classifications of pathogenicity
Select item 42901	NM_000257.4(MYH7):c.2389G>A (p.Ala797Thr)	LOC126861898, MYH7 (A797T)	Single nucleotide variant (missense variant)	Myosin storage myopathy +18 more	GPathogenic/Likely pathogenic
Select item 164334	NM_000257.4(MYH7):c.2358G>T (p.Thr786=)	LOC126861898, MYH7	Single nucleotide variant (synonymous variant)	Cardiomyopathy	GBenign FDA Recognized database
Select item 42896	NM_000257.4(MYH7):c.2349C>T (p.Arg783=)	LOC126861898, MYH7	Single nucleotide variant (synonymous variant)	Dilated Cardiomyopathy, Dominant +9 more	GBenign/Likely benign

ClinVar