| | LOC126861897, MHRT +1 more | Microsatellite (non-coding transcript variant +1 more) | MYH7-related skeletal myopathy | |
| | LOC126861897, MHRT +1 more (E1669del) | Deletion (non-coding transcript variant +1 more) | Hypertrophic cardiomyopathy +1 more | |
| | LOC126861897, MHRT +1 more (R1662P) | Single nucleotide variant (non-coding transcript variant +1 more) | MYH7-related disorder +1 more | |
| | LOC126861897, MHRT +1 more (L1646P) | Single nucleotide variant (non-coding transcript variant +1 more) | Hypertrophic cardiomyopathy +1 more | |
| | LOC126861897, MHRT +1 more (A1636P) | Single nucleotide variant (non-coding transcript variant +1 more) | MYH7-related skeletal myopathy | |
| | LOC126861897, MHRT +1 more (K1617del) | Microsatellite (inframe_deletion +1 more) | not provided +3 more | GPathogenic/Likely pathogenic |
| | LOC126861897, MHRT +1 more (L1612P) | Single nucleotide variant (non-coding transcript variant +1 more) | Qualitative or quantitative defects of beta-myosin heavy chain (MYH7) +1 more | |
| | LOC126861897, MHRT +1 more (R1608P) | Single nucleotide variant (non-coding transcript variant +1 more) | MYH7-related skeletal myopathy | |
| | LOC126861897, MHRT +1 more (T1599P) | Single nucleotide variant (non-coding transcript variant +1 more) | MYH7-related skeletal myopathy | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Microsatellite (splice acceptor variant +1 more) | Cardiomyopathy +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | MYH7-related skeletal myopathy | |