"Diagnostic Laboratory, Department of Genetics, University Medical Cen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1174659	NM_002471.4(MYH6):c.5129A>T (p.Glu1710Val)	LOC126861896, MYH6 (E1710V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 227592	NM_002471.4(MYH6):c.5112G>A (p.Ala1704=)	LOC126861896, MYH6	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 14 +4 more	GBenign/Likely benign
Select item 861577	NM_002471.4(MYH6):c.5026G>A (p.Val1676Met)	LOC126861896, MYH6 (V1676M)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 44529	NM_002471.4(MYH6):c.4986G>A (p.Ala1662=)	LOC126861896, MYH6	Single nucleotide variant (synonymous variant)	Cardiomyopathy +4 more	GBenign/Likely benign
Select item 179576	NM_002471.4(MYH6):c.4960-9G>A	LOC126861896, MYH6	Single nucleotide variant (intron variant)	Atrial septal defect 3 +7 more	GBenign
Select item 44526	NM_002471.4(MYH6):c.4914T>C (p.Ala1638=)	LOC126861896, MYH6	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +3 more	GBenign
Select item 178065	NM_002471.4(MYH6):c.4905C>T (p.Asn1635=)	LOC126861896, MYH6	Single nucleotide variant (synonymous variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 239176	NM_002471.4(MYH6):c.4651-3C>A	MYH6, LOC126861896	Single nucleotide variant (intron variant)	not provided +2 more	GUncertain significance

ClinVar