C2750466[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2582542	NM_002471.4(MYH6):c.3946G>A (p.Asp1316Asn)	MYH6 (D1316N)	Single nucleotide variant (missense variant)	MYH6-related cardiac defects +2 more	GUncertain significance
Select item 574886	NM_002471.4(MYH6):c.2615G>A (p.Arg872His)	MYH6 (R872H)	Single nucleotide variant (missense variant)	not provided +5 more	GUncertain significance
Select item 36627	NM_002471.4(MYH6):c.1753G>A (p.Gly585Ser)	MYH6 (G585S)	Single nucleotide variant (missense variant)	not provided +8 more	GUncertain significance
Select item 1024279	NM_002471.4(MYH6):c.1088T>C (p.Met363Thr)	MYH6 (M363T)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +5 more	GUncertain significance
Select item 656196	NM_002471.4(MYH6):c.864C>G (p.Tyr288Ter)	MYH6 (Y288*)	Single nucleotide variant (nonsense)	not provided +5 more	GUncertain significance
Select item 1032062	NM_002471.4(MYH6):c.493A>T (p.Met165Leu)	LOC114827851, MYH6 (M165L)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +6 more	GUncertain significance
Select item 2441788	NM_002471.4(MYH6):c.478A>G (p.Asn160Asp)	LOC114827851, MYH6 (N160D)	Single nucleotide variant (missense variant)	Atrial septal defect 3 +2 more	GUncertain significance

ClinVar