MYH7 and left ventricular noncompaction: Table S4 contains lists of rare genetic variants of further cardiomyopathy associated genes in all probands (frequency in Exac database less than 0.00001). Just the variant of MYH7 (NM_000257.3) c.4679G > C, p.(Arg1560Pro) in proband 4 could be relevant in a patient with LVNC. However, it was not present in other members of the family tested (II 1, 3, 4; III 1, 2) (Figure 1) and did not co-segregate with the phenotype of LVNC.