Genetic variants in further genes with established association for DCM/LVNC accounted for the rest of the cases: variants in genes coding for sarcomere proteins (e.g., MYH7, MYBPC3, and TNNT2), nuclear envelope proteins (e.g., LMNA), or the cytoskeleton (FLNC) (Supplementary Figure S2). Here, MYH7 is linked to familial dilated cardiomyopathy.