| | | Single nucleotide variant (genic upstream transcript variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (5 prime UTR variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (5 prime UTR variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (5 prime UTR variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (5 prime UTR variant) | not provided +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | MEGF10-related myopathy | |
| | | Deletion (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | MEGF10-related myopathy +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not specified | |
| | | Single nucleotide variant (intron variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Duplication (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | MEGF10-related myopathy | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (missense variant) | MEGF10-related myopathy +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (missense variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (synonymous variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (missense variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (synonymous variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (synonymous variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (synonymous variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (missense variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (intron variant) | not specified +1 more | |
| | | Single nucleotide variant (intron variant) | MEGF10-related myopathy +2 more | |
| | | Single nucleotide variant (intron variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (intron variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (intron variant) | MEGF10-related myopathy | |
| | | Deletion (intron variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (intron variant) | MEGF10-related myopathy | |
| | | Insertion (intron variant) | MEGF10-related myopathy +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (synonymous variant) | MEGF10-related myopathy +1 more | |
| | | Single nucleotide variant (synonymous variant) | MEGF10-related myopathy | |
| | | Microsatellite (frameshift variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (missense variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (synonymous variant) | not specified | |
| | | Single nucleotide variant (missense variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (missense variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (synonymous variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (synonymous variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (synonymous variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (missense variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (missense variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (missense variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (missense variant) | MEGF10-related myopathy | |
| | | Indel (nonsense) | MEGF10-related myopathy | |
| | | Single nucleotide variant (missense variant) | MEGF10-related myopathy +1 more | |
| | | Single nucleotide variant (synonymous variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (missense variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (missense variant) | MEGF10-related myopathy +1 more | |
| | | Duplication (frameshift variant) | not provided | |
| | | Single nucleotide variant (intron variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (intron variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (intron variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (intron variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (intron variant) | not specified +2 more | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Microsatellite (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Deletion (intron variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (intron variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (intron variant) | not specified +1 more | |
| | | Single nucleotide variant (intron variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (intron variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (nonsense) | MEGF10-related myopathy | |
| | | Single nucleotide variant (nonsense) | MEGF10-related myopathy | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | MEGF10-related myopathy +2 more | |
| | | Single nucleotide variant (missense variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (missense variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (missense variant) | MEGF10-related myopathy | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | EBV-positive nodal T- and NK-cell lymphoma | |
| | | Single nucleotide variant (synonymous variant) | MEGF10-related myopathy +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Congenital myopathy 10b, mild variant +1 more | GConflicting classifications of pathogenicity |