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Family K32326 pedigree. The gender of family members is masked for confidentiality. Black symbols represent patients with WPW and a gray symbol represents the patient with a diagnosis of SVT (Patient 1:2): autosomal dominant inheritance, with incomplete penetrance, is the most likely genetic model. Only participants in the study for whom DNA is available for analysis are numbered. +: Positive for MYH6 c.5653G>A, p.Glu1885Lys; −: Negative for MYH6 c.5653G>A, p.Glu1885Lys.
