613690.G.2

Lebanon

Hypertrophic cardiomyopathy; Sudden cardiac death;

Yes

Variant Name	Allele Count	Allele Frequency	Associated Disease	Associated Gene
NM_000363.5:c.61C>T	7		Cardiomyopathy, Familial Hypertrophic 7

Pedigree with 19 affected members; 7 molecularly characterized