| | | Single nucleotide variant (3 prime UTR variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (3 prime UTR variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (3 prime UTR variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (3 prime UTR variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (3 prime UTR variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (3 prime UTR variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (3 prime UTR variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (3 prime UTR variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (3 prime UTR variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (3 prime UTR variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (3 prime UTR variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (3 prime UTR variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (3 prime UTR variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (3 prime UTR variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (3 prime UTR variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (3 prime UTR variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (3 prime UTR variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (3 prime UTR variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (missense variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (synonymous variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Spinocerebellar ataxia type 11 +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (missense variant) | TTBK2-related condition +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | TTBK2-related condition +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Spinocerebellar ataxia type 11 +2 more | |
| | | Single nucleotide variant (missense variant) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Spinocerebellar ataxia type 11 +1 more | |
| | | Single nucleotide variant (missense variant) | Spinocerebellar ataxia type 11 +1 more | |
| | | Single nucleotide variant (missense variant) | TTBK2-related condition +3 more | |
| | | Single nucleotide variant (synonymous variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (missense variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | Spinocerebellar ataxia type 11 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Spinocerebellar ataxia type 11 +1 more | |
| | | Single nucleotide variant (missense variant) | Spinocerebellar ataxia type 11 +2 more | |
| | | Single nucleotide variant (synonymous variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (missense variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (missense variant) | TTBK2-related condition +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Spinocerebellar ataxia type 11 +1 more | |
| | | Single nucleotide variant (missense variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | | Single nucleotide variant (intron variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Spastic ataxia +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (missense variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (missense variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (missense variant) | not specified +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Spinocerebellar ataxia type 11 +3 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (intron variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (5 prime UTR variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (5 prime UTR variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (5 prime UTR variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (5 prime UTR variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (5 prime UTR variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (5 prime UTR variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (5 prime UTR variant) | Spinocerebellar ataxia type 11 | |
| | | Single nucleotide variant (genic upstream transcript variant) | Spinocerebellar ataxia type 11 | |