"Institute of Human Genetics, University of Wuerzburg"[submitter] AND - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3255532	NM_002471.4(MYH6):c.5569G>C (p.Glu1857Gln)	MYH6 (E1857Q)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 2	Gnot provided
Select item 3255538	NM_002471.4(MYH6):c.5566-1G>C	MYH6	Single nucleotide variant (splice acceptor variant)	Hypertrophic cardiomyopathy 2	Gnot provided
Select item 1329250	NM_002471.4(MYH6):c.5566-2A>C	MYH6	Single nucleotide variant (splice acceptor variant)	Cardiomyopathy	GBenign
Select item 3255544	NM_002471.4(MYH6):c.5566-19C>T	MYH6	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy 2	Gnot provided
Select item 36628	NM_002471.4(MYH6):c.3979-8del	MYH6	Deletion (intron variant)	Hypertrophic cardiomyopathy 14 +6 more	GConflicting classifications of pathogenicity
Select item 1704208	NM_002471.4(MYH6):c.2419G>C (p.Val807Leu)	MYH6 (V807L)	Single nucleotide variant (missense variant)	Cardiomyopathy	GUncertain significance

ClinVar