"Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, E - 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 14120	NM_000257.4(MYH7):c.2609G>A (p.Arg870His)	LOC126861898, MYH7 (R870H)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy	GPathogenic FDA Recognized database
Select item 1174821	NM_000257.4(MYH7):c.2562G>T (p.Glu854Asp)	LOC126861898, MYH7 (E854D)	Single nucleotide variant (missense variant)	Cardiomyopathy	GUncertain significance
Select item 418361	NM_000257.4(MYH7):c.2455C>T (p.Arg819Trp)	LOC126861898, MYH7 (R819W)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy +2 more	GConflicting classifications of pathogenicity
Select item 42896	NM_000257.4(MYH7):c.2349C>T (p.Arg783=)	LOC126861898, MYH7	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 1 +9 more	GBenign/Likely benign
Select item 265252	NM_000257.4(MYH7):c.2334C>G (p.Asp778Glu)	LOC126861898, MYH7 (D778E)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +3 more	GPathogenic/Likely pathogenic
Select item 42894	NM_000257.4(MYH7):c.2334C>T (p.Asp778=)	LOC126861898, MYH7	Single nucleotide variant (synonymous variant)	Myosin storage myopathy +8 more	GConflicting classifications of pathogenicity

ClinVar