Other variants found were associated with a neuromuscular disease (<i>SMN1, MYH2,</i> and <i>LMNA</i> genes), neurodegenerative disorder (<i>TSPOAP1, CACNA1A</i>, <i>ALS2, and SCN2A</i> genes), multisystemic disease (<i>EPG5, NKX1-2, ATRX,</i> and <i>ABCC6</i> genes), and one in an isolated cardiomyopathy causing gene (<i>MYBPC3</i>).