Table 1.

Genotyping of G+LVH‐ and G+LVH+

Causal Gene Mutation, n (%)	G+LVH‐ (n=45)	G+LVH+ (n=5)
MYBPC3	27 (60)	3 (60)
MYH7	9 (20)	1 (20)
TNNI3	5 (11.1)	0 (0)
TNNT2	1 (2.2)	1 (20)
TPM1	1 (2.2)	0 (0)
CSRP3	1 (2.2)	0 (0)
MYL2	1 (2.2)	0 (0)

CSRP3 indicates cysteine and glycine‐rich protein 3; G+LVH‐, genotype‐positive, left ventricular hypertrophy‐negative; G+LVH+, genotype‐positive, left ventricular hypertrophy‐positive; MYBPC3, myosin binding protein C; MYH7, β‐myosin heavy chain; MYL2, myosin regulatory light chain; TNNI3, cardiac troponin I; TNNT2, cardiac troponin T; and TPM1, α‐tropomyosin 1.