C3715165[trait identifier] AND "Phosphorus, Inc."[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 42658	NM_000256.3(MYBPC3):c.2800C>T (p.Leu934=)	MYBPC3	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +5 more	GConflicting classifications of pathogenicity
Select item 8608	NM_000256.3(MYBPC3):c.1624G>C (p.Glu542Gln)	MYBPC3 (E542Q)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +8 more	GPathogenic
Select item 180940	NM_000256.3(MYBPC3):c.1471G>A (p.Val491Met)	MYBPC3 (V491M)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +6 more	GUncertain significance
Select item 164117	NM_000256.3(MYBPC3):c.1445C>T (p.Ala482Val)	MYBPC3 (A482V)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +6 more	GUncertain significance
Select item 42792	NM_000256.3(MYBPC3):c.772G>A (p.Glu258Lys)	MYBPC3 (E258K)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +6 more	GPathogenic/Likely pathogenic
Select item 36613	NM_000256.3(MYBPC3):c.529C>T (p.Arg177Cys)	MYBPC3 (R177C)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +6 more	GConflicting classifications of pathogenicity

ClinVar