| | | Single nucleotide variant (missense variant) | Cardiomyopathy +8 more | |
| | | Single nucleotide variant (missense variant) | not provided +9 more | |
| | | Single nucleotide variant (missense variant) | Myopathy, myosin storage, autosomal recessive +6 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +9 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +9 more | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy +9 more | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy +9 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +8 more | |
| | | Single nucleotide variant (missense variant) | Dilated Cardiomyopathy, Dominant +10 more | |
| | | Single nucleotide variant (missense variant) | Primary dilated cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 1 +8 more | |
| | | Single nucleotide variant (intron variant) | not provided +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Myosin storage myopathy +6 more | |
| | | Single nucleotide variant (missense variant) | Primary dilated cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +10 more | |
| | | Indel (missense variant) | Cardiovascular phenotype +10 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +7 more | |
| | | Single nucleotide variant (missense variant) | not provided +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +7 more | |
| | | Single nucleotide variant (missense variant) | Myosin storage myopathy | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +9 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy +9 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy | |
| | LOC126861897, MYH7 (L1769M) | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy | |
| | LOC126861897, MYH7 (A1763T) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +11 more | |
| | | Single nucleotide variant (intron variant) | not specified +8 more | |
| | LOC126861897, MYH7 (E1743D) | Single nucleotide variant (missense variant) | Cardiomyopathy +9 more | |
| | LOC126861897, MHRT +1 more (S1735T) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided +9 more | |
| | LOC126861897, MHRT +1 more (D1731V) | Single nucleotide variant (non-coding transcript variant +1 more) | Hypertrophic cardiomyopathy +8 more | |
| | LOC126861897, MHRT +1 more | Single nucleotide variant (synonymous variant +1 more) | Myopathy, myosin storage, autosomal recessive +6 more | |
| | LOC126861897, MHRT +1 more (R1712Q) | Single nucleotide variant (non-coding transcript variant +1 more) | Hypertrophic cardiomyopathy | |
| | LOC126861897, MHRT +1 more | Single nucleotide variant (non-coding transcript variant +1 more) | Cardiomyopathy | |
| | LOC126861897, MHRT +1 more (R1689H) | Single nucleotide variant (non-coding transcript variant +1 more) | Hypertrophic cardiomyopathy +9 more | |
| | LOC126861897, MHRT +1 more (R1689C) | Single nucleotide variant (non-coding transcript variant +1 more) | Cardiovascular phenotype +9 more | |
| | LOC126861897, MHRT +1 more (N1679K) | Single nucleotide variant (non-coding transcript variant +1 more) | Hypertrophic cardiomyopathy +8 more | |
| | LOC126861897, MHRT +1 more (R1677H) | Single nucleotide variant (non-coding transcript variant +1 more) | Hypertrophic cardiomyopathy +11 more | |
| | LOC126861897, MHRT +1 more (R1676W) | Single nucleotide variant (non-coding transcript variant +1 more) | Hypertrophic cardiomyopathy +9 more | |
| | LOC126861897, MHRT +1 more (A1660E) | Single nucleotide variant (non-coding transcript variant +1 more) | Hypertrophic cardiomyopathy +8 more | |
| | LOC126861897, MHRT +1 more (D1652Y) | Single nucleotide variant (missense variant) | not provided +9 more | |
| | LOC126861897, MHRT +1 more | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy +6 more | |
| | LOC126861897, MHRT +1 more | Single nucleotide variant (intron variant) | Myopathy, myosin storage, autosomal recessive +7 more | |
| | LOC126861897, MHRT +1 more | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 1 +6 more | |
| | MHRT, LOC126861897 +1 more (A1639V) | Single nucleotide variant (non-coding transcript variant +1 more) | MYH7-related disorder +9 more | |
| | LOC126861897, MHRT +1 more (M1635T) | Single nucleotide variant (non-coding transcript variant +1 more) | Hypertrophic cardiomyopathy +9 more | |
| | LOC126861897, MHRT +1 more (R1634H) | Single nucleotide variant (non-coding transcript variant +1 more) | Hypertrophic cardiomyopathy +10 more | |
| | LOC126861897, MHRT +1 more (A1632T) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided +10 more | |
| | LOC126861897, MHRT +1 more (L1612V) | Single nucleotide variant (non-coding transcript variant +1 more) | Myosin storage myopathy +6 more | |
| | LOC126861897, MHRT +1 more (A1611S) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided +9 more | |
| | MHRT, LOC126861897 +1 more (S1607G) | Single nucleotide variant (non-coding transcript variant +1 more) | Congenital myopathy with fiber type disproportion +7 more | |
| | LOC126861897, MHRT +1 more (A1603T) | Single nucleotide variant (non-coding transcript variant +1 more) | Cardiomyopathy +9 more | |
| | LOC126861897, MHRT +1 more | Single nucleotide variant (non-coding transcript variant +1 more) | Myosin storage myopathy +13 more | |
| | LOC126861897, MHRT +1 more (R1592Q) | Single nucleotide variant (non-coding transcript variant +1 more) | Dilated cardiomyopathy 1S +7 more | |
| | LOC126861897, MHRT +1 more (L1591Q) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided +9 more | |
| | LOC126861897, MHRT +1 more (A1586T) | Single nucleotide variant (non-coding transcript variant +1 more) | Conduction disorder of the heart +8 more | |
| | LOC126861897, MHRT +1 more (R1560Q) | Single nucleotide variant (non-coding transcript variant +1 more) | Hypertrophic cardiomyopathy +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 1 +9 more | |
| | | Single nucleotide variant (missense variant) | Myopathy, myosin storage, autosomal recessive +7 more | |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy +9 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Cardiomyopathy | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Myopathy, myosin storage, autosomal recessive +6 more | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy +8 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy +9 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Cardiovascular phenotype +8 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Dilated cardiomyopathy 1S +9 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Cardiomyopathy | |
| | | Single nucleotide variant (intron variant) | Dilated cardiomyopathy 1S +7 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Cardiomyopathy +13 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Hypertrophic cardiomyopathy +10 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Hypertrophic cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy | |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy +8 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +10 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy +8 more | |
| | | Single nucleotide variant (synonymous variant) | Myosin storage myopathy +11 more | |
| | | Single nucleotide variant (intron variant) | Cardiomyopathy +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +8 more | |
| | | Single nucleotide variant (synonymous variant) | Congenital myopathy with fiber type disproportion +8 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Myosin storage myopathy +11 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 1 +8 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +9 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | not provided +10 more | |
| | | Single nucleotide variant (missense variant) | Myosin storage myopathy +9 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +9 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy | |
| | | Single nucleotide variant (intron variant) | not provided +8 more | |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy 1 +9 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +9 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Myosin storage myopathy +12 more | |
| | | Single nucleotide variant (missense variant) | not provided +9 more | |