Furthermore, the Sanger sequencing analysis with the BMP10-specific primers presented in Table 3 unveiled that merely the nonsense variation of chr2:69,098,325C > T (GRCh37.p13/hg19: NC_000002.11), equal to chr2:68,861,113C > T (GRCh38.p14/hg38: NC_000002.12) or NM_014482.3: c.166C > T;p.(Gln56*), in BMP10 was confirmed and validated to co-segregate with DCM in the whole family, with complete penetrance, being shared by all affected and none of the unaffected members. This evidence concerns the gene BMP10 and familial dilated cardiomyopathy.