"Division of Medical Genetics, University of Washington"[submitter] AN - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 36604	NM_000256.3(MYBPC3):c.2308G>A (p.Asp770Asn)	MYBPC3 (D770N)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +7 more	GConflicting classifications of pathogenicity
Select item 164091	NM_000256.3(MYBPC3):c.1999_2000delinsG (p.Leu667fs)	MYBPC3	Indel	Cardiovascular phenotype +4 more	GPathogenic/Likely pathogenic