C1842160[trait identifier] AND "Laboratory of Medical Genetics, Nation - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 143214	NM_000257.4(MYH7):c.4937T>C (p.Leu1646Pro)	LOC126861897, MHRT +1 more (L1646P)	Single nucleotide variant (non-coding transcript variant +1 more)	Myosin storage myopathy +1 more	GPathogenic
Select item 312903	NM_000257.4(MYH7):c.3035C>A (p.Ala1012Asp)	MYH7 (A1012D)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +9 more	GConflicting classifications of pathogenicity