"Suma Genomics"[submitter] AND "MYO1H"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1341353	NM_001101421.3(MYO1H):c.1784del	MYO1H	Deletion	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction	GLikely benign
Select item 1341354	NM_001101421.4(MYO1H):c.3067AAAAAT[1] (p.1023KN[1])	MYO1H	Microsatellite (inframe_deletion)	Central hypoventilation syndrome, congenital, 2, and autonomic dysfunction	GLikely benign