| | | Single nucleotide variant (5 prime UTR variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (intron variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (intron variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Duplication (intron variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (intron variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | not specified +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | LOC126860282, MYOM2 (Y927C) | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | LOC126860282, MYOM2 (A938T) | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | MYOM2, LOC126860282 (E954G) | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (intron variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (intron variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder +1 more | |
| | | Single nucleotide variant (intron variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (intron variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (intron variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (missense variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (intron variant) | MYOM2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | MYOM2-related disorder | |