| | | Single nucleotide variant (synonymous variant +2 more) | TWNK-related disorder | |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided +1 more | |
| | | Single nucleotide variant (missense variant +2 more) | TWNK-related disorder | |
| | | Single nucleotide variant (missense variant +2 more) | TWNK-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | TWNK-related disorder | |
| | | Single nucleotide variant (synonymous variant +2 more) | TWNK-related disorder +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | TWNK-related disorder | |
| | | Single nucleotide variant (missense variant +2 more) | TWNK-related disorder +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +2 more) | TWNK-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | TWNK-related disorder | |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | TWNK-related disorder +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | TWNK-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary spastic paraplegia +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not specified +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | TWNK-related disorder +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | TWNK-related disorder +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | TWNK-related disorder +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | not provided +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | not provided +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | TWNK-related disorder +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | TWNK-related disorder +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | Autosomal recessive cerebellar ataxia +6 more | GConflicting classifications of pathogenicity |