613690.G.3

Country

Lebanon

HPO Terms

Hypertrophic cardiomyopathy; Sudden cardiac death;
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Family History

Yes

Parental Consanguinity

No

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_000363.5:c.61C>T3

Remarks

Pedigree with 10 affected members; 3 molecularly characterized
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