"Biesecker Lab/Clinical Genomics Section, National Institutes of Healt - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 44541	NM_002471.4(MYH6):c.622G>A (p.Asp208Asn)	LOC114827851, MYH6 (D208N)	Single nucleotide variant (missense variant)	not provided +5 more	GBenign/Likely benign
Select item 191722	NM_002471.4(MYH6):c.421G>A (p.Ala141Thr)	LOC114827851, MYH6 (A141T)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 44455	NM_002471.4(MYH6):c.166G>A (p.Gly56Arg)	LOC114827851, MYH6 (G56R)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign
Select item 191723	NM_002471.4(MYH6):c.121G>A (p.Asp41Asn)	LOC114827851, MYH6 (D41N)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 191724	NM_002471.4(MYH6):c.115G>A (p.Val39Met)	LOC114827851, MYH6 (V39M)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +6 more	GConflicting classifications of pathogenicity
Select item 164258	NM_002471.4(MYH6):c.86G>A (p.Arg29Gln)	LOC114827851, MYH6 (R29Q)	Single nucleotide variant (missense variant)	Cardiomyopathy +4 more	GBenign

ClinVar