| | | Single nucleotide variant (synonymous variant +1 more) | SOX10-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | SOX10-related disorder +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | SOX10-related disorder +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | PCWH syndrome +5 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | SOX10-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | SOX10-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | PCWH syndrome +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | SOX10-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | SOX10-related disorder +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | SOX10-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | SOX10-related disorder +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | SOX10-related disorder +1 more | GConflicting classifications of pathogenicity |
| | | Duplication (frameshift variant +1 more) | SOX10-related disorder | |
| | | Deletion (frameshift variant +1 more) | SOX10-related disorder | |
| | | Duplication (frameshift variant +1 more) | SOX10-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | SOX10-related disorder | |
| | | Single nucleotide variant (intron variant) | SOX10-related disorder +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Waardenburg syndrome type 2E +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Hearing impairment +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +3 more | |
| | | Duplication (frameshift variant +1 more) | SOX10-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense +1 more) | SOX10-related disorder +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | PCWH syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | SOX10-related disorder | |
| | | Duplication (frameshift variant +1 more) | SOX10-related disorder | |
| | | Single nucleotide variant (intron variant) | SOX10-related disorder +1 more | |