C3495498[trait identifier] AND "Genomic Diagnostic Laboratory, Divisio - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 43020	NM_000257.4(MYH7):c.4472C>G (p.Ser1491Cys)	MHRT, MYH7 (S1491C)	Single nucleotide variant (missense variant)	Cardiomyopathy	GBenign FDA Recognized database
Select item 42956	NM_000257.4(MYH7):c.3337-4dup	MYH7	Duplication	Cardiomyopathy	GBenign FDA Recognized database
Select item 42946	NM_000257.4(MYH7):c.3153G>A (p.Ala1051=)	MYH7	Single nucleotide variant (synonymous variant)	Cardiomyopathy	GBenign FDA Recognized database
Select item 37375	NM_000257.4(MYH7):c.77C>T (p.Ala26Val)	MYH7 (A26V)	Single nucleotide variant (missense variant)	Cardiomyopathy	GBenign FDA Recognized database

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