| | | Single nucleotide variant (3 prime UTR variant +1 more) | not specified +1 more | |
| | | Deletion (3 prime UTR variant +1 more) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | DMD-related disorder | |
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | |
| | | Single nucleotide variant (stop lost +1 more) | Becker muscular dystrophy +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (missense variant) | Duchenne muscular dystrophy +6 more | |
| | | Single nucleotide variant (intron variant) | Duchenne muscular dystrophy +3 more | |
| | | Single nucleotide variant (intron variant) | DMD-related disorder | |
| | | Single nucleotide variant (intron variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | DMD-related disorder +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | DMD-related disorder +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | DMD-related disorder +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (synonymous variant) | DMD-related disorder | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not specified +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Duchenne muscular dystrophy +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Duchenne muscular dystrophy +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Duchenne muscular dystrophy +2 more | |
| | | Single nucleotide variant (synonymous variant) | Duchenne muscular dystrophy +4 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | DMD-related disorder | |
| | | Single nucleotide variant (intron variant) | DMD-related disorder | |
| | | Single nucleotide variant (missense variant) | Duchenne muscular dystrophy +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Duchenne muscular dystrophy +3 more | |
| | | Single nucleotide variant (synonymous variant) | Duchenne muscular dystrophy +5 more | |
| | | Single nucleotide variant (intron variant) | DMD-related disorder | |
| | | Single nucleotide variant (synonymous variant) | Duchenne muscular dystrophy +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Duchenne muscular dystrophy +4 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Duchenne muscular dystrophy +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | Duchenne muscular dystrophy +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Duchenne muscular dystrophy +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Duchenne muscular dystrophy +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +3 more | |
| | | Single nucleotide variant (intron variant) | Duchenne muscular dystrophy +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Primary familial dilated cardiomyopathy +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Duchenne muscular dystrophy +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Duchenne muscular dystrophy +4 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +3 more | |
| | | Single nucleotide variant (missense variant) | Duchenne muscular dystrophy +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Duchenne muscular dystrophy +1 more | |
| | | Single nucleotide variant (intron variant) | Duchenne muscular dystrophy +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Duchenne muscular dystrophy +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | DMD-related disorder +2 more | |
| | | Single nucleotide variant (synonymous variant) | Duchenne muscular dystrophy +4 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (missense variant) | Duchenne muscular dystrophy +4 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +5 more | |
| | | Single nucleotide variant (synonymous variant) | Duchenne muscular dystrophy +2 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 3B +5 more | |
| | | Single nucleotide variant (missense variant) | DMD-related disorder +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | DMD-related disorder | |
| | | Single nucleotide variant (missense variant) | not specified +3 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (missense variant) | not specified +3 more | |
| | | Single nucleotide variant (intron variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | DMD-related disorder +1 more | |
| | | Single nucleotide variant (intron variant) | Dilated cardiomyopathy 3B +3 more | |
| | | Single nucleotide variant (splice donor variant) | not provided +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Duchenne muscular dystrophy +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | DMD-related disorder +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | DMD-related disorder | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 3B +4 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +4 more | |
| | | Duplication (frameshift variant) | DMD-related disorder | |
| | | Single nucleotide variant (missense variant) | Duchenne muscular dystrophy +2 more | |
| | | Single nucleotide variant (synonymous variant) | Duchenne muscular dystrophy +1 more | |
| | | Microsatellite (intron variant) | Duchenne muscular dystrophy +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Duchenne muscular dystrophy +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | not specified +3 more | |
| | | Single nucleotide variant (intron variant) | Duchenne muscular dystrophy +2 more | |
| | | Single nucleotide variant (missense variant) | Duchenne muscular dystrophy +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | DMD-related disorder +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Dilated cardiomyopathy 3B +4 more | |
| | | Single nucleotide variant (synonymous variant) | DMD-related disorder +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | DMD-related disorder +2 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (missense variant) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Duchenne muscular dystrophy +4 more | |
| | | Single nucleotide variant (missense variant) | DMD-related disorder | |
| | | Single nucleotide variant (synonymous variant) | Duchenne muscular dystrophy +2 more | |
| | | Single nucleotide variant (intron variant) | not provided +3 more | |