| | | Deletion | Dilated cardiomyopathy 1S | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1S | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (splice donor variant) | MYH7-related disorder | |
| | LOC126861897, MYH7 (D1761fs) | Deletion (frameshift variant) | MYH7-related disorder | |
| | | Single nucleotide variant (splice acceptor variant) | MYH7-related disorder | |
| | | Single nucleotide variant (nonsense) | MYH7-related disorder | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Myosin storage myopathy | |
| | | Deletion | not specified | |
| | | Duplication (splice acceptor variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | LOC126861898, MYH7 (L796P) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | LOC126861897, MHRT +1 more (S1630R) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | LOC126861897, MHRT +1 more (V1643I) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | LOC126861897, MHRT +1 more (L1681P) | Single nucleotide variant (non-coding transcript variant +1 more) | MYH7-related skeletal myopathy | |
| | LOC126861897, MHRT +1 more | Single nucleotide variant (non-coding transcript variant +1 more) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | LOC126861898, MYH7 (R845G) | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 2 | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 2 | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 1 | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 1 | |
| | | Deletion (frameshift variant) | not provided | |
| | LOC126861897, MHRT +1 more (R1588P) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Deletion | Hypertrophic cardiomyopathy | |
| | | Duplication | Hypertrophic cardiomyopathy | |
| | | Duplication | Hypertrophic cardiomyopathy | |
| | | Duplication | Hypertrophic cardiomyopathy | |
| | | Duplication | Hypertrophic cardiomyopathy | |
| | | Deletion | Hypertrophic cardiomyopathy | |
| | | Deletion | Hypertrophic cardiomyopathy | |
| | | Deletion | Hypertrophic cardiomyopathy | |
| | LOC126861897, MHRT +2 more (S1648fs) | Deletion (non-coding transcript variant +1 more) | Hypertrophic cardiomyopathy 1 | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 1 | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1S +3 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1S | |
| | | Deletion (frameshift variant) | not specified | |
| | LOC126861897, MHRT +1 more (L1723P) | Single nucleotide variant (non-coding transcript variant +1 more) | Myosin storage myopathy | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | LOC126861897, MHRT +1 more (N1720S) | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | LOC126861897, MHRT +1 more (Q1704K) | Single nucleotide variant (non-coding transcript variant +1 more) | Cardiovascular phenotype | |
| | | Single nucleotide variant (splice donor variant) | Cardiovascular phenotype | |
| | LOC126861897, MHRT +1 more | Single nucleotide variant (non-coding transcript variant +1 more) | Cardiovascular phenotype | |
| | LOC126861897, MHRT +1 more | Single nucleotide variant (non-coding transcript variant +1 more) | Cardiovascular phenotype | |
| | LOC126861897, MHRT +1 more (K1557N) | Single nucleotide variant (non-coding transcript variant +1 more) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | LOC126861898, MYH7 (I814K) | Indel (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | LOC126861897, MHRT +1 more | Single nucleotide variant (non-coding transcript variant +1 more) | Cardiovascular phenotype | |
| | LOC126861897, MHRT +2 more | Deletion | Primary dilated cardiomyopathy | |
| | | Single nucleotide variant (nonsense) | Cardiomyopathy | |
| | LOC126861898, MYH7 (M877L) | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 1 | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Single nucleotide variant (splice acceptor variant) | Cardiomyopathy | |
| | | Single nucleotide variant (intron variant) | Cardiomyopathy | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy | |
| | MHRT, LOC126861897 +1 more | Single nucleotide variant (non-coding transcript variant +1 more) | Cardiomyopathy | |
| | LOC126861897, MHRT +1 more | Single nucleotide variant (intron variant) | Cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | MHRT, LOC126861897 +1 more (E1703G) | Single nucleotide variant (non-coding transcript variant +1 more) | Cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Deletion (nonsense) | Cardiomyopathy | |
| | LOC126861897, MYH7 (K1756R) | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Duplication (frameshift variant) | Cardiomyopathy | |
| | LOC126861897, MHRT +1 more (V1593L) | Single nucleotide variant (non-coding transcript variant +1 more) | Cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |