| | | Single nucleotide variant (3 prime UTR variant) | Early-onset generalized limb-onset dystonia | |
| | | Single nucleotide variant (3 prime UTR variant) | Early-onset generalized limb-onset dystonia | |
| | | Single nucleotide variant (3 prime UTR variant) | Early-onset generalized limb-onset dystonia | |
| | | Single nucleotide variant (3 prime UTR variant) | Early-onset generalized limb-onset dystonia | |
| | | Single nucleotide variant (3 prime UTR variant) | Early-onset generalized limb-onset dystonia | |
| | | Single nucleotide variant (3 prime UTR variant) | Early-onset generalized limb-onset dystonia | |
| | | Single nucleotide variant (3 prime UTR variant) | Early-onset generalized limb-onset dystonia | |
| | | Microsatellite (3 prime UTR variant) | Early-onset generalized limb-onset dystonia | |
| | | Single nucleotide variant (3 prime UTR variant) | Early-onset generalized limb-onset dystonia | |
| | | Single nucleotide variant (3 prime UTR variant) | Early-onset generalized limb-onset dystonia | |
| | | Single nucleotide variant (3 prime UTR variant) | Early-onset generalized limb-onset dystonia | |
| | | Deletion (3 prime UTR variant) | Early-onset generalized limb-onset dystonia | |
| | | Single nucleotide variant (3 prime UTR variant) | Early-onset generalized limb-onset dystonia | |
| | | Single nucleotide variant (3 prime UTR variant) | Early-onset generalized limb-onset dystonia | |
| | | Single nucleotide variant (3 prime UTR variant) | Early-onset generalized limb-onset dystonia | |
| | | Single nucleotide variant (3 prime UTR variant) | Early-onset generalized limb-onset dystonia | |
| | | Deletion (3 prime UTR variant) | Early-onset generalized limb-onset dystonia | |
| | | Single nucleotide variant (3 prime UTR variant) | Early-onset generalized limb-onset dystonia | |
| | | Insertion (3 prime UTR variant) | Early-onset generalized limb-onset dystonia | |
| | | Single nucleotide variant (3 prime UTR variant) | Early-onset generalized limb-onset dystonia | |
| | | Deletion (3 prime UTR variant) | Early-onset generalized limb-onset dystonia | |
| | | Single nucleotide variant (3 prime UTR variant) | Early-onset generalized limb-onset dystonia | |
| | | Single nucleotide variant (3 prime UTR variant) | Early-onset generalized limb-onset dystonia | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Early-onset generalized limb-onset dystonia | |
| | | Single nucleotide variant (3 prime UTR variant) | Early-onset generalized limb-onset dystonia +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Dystonic disorder +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Early-onset generalized limb-onset dystonia | |
| | | Single nucleotide variant (3 prime UTR variant) | Early-onset generalized limb-onset dystonia | |
| | | Single nucleotide variant (3 prime UTR variant) | Early-onset generalized limb-onset dystonia | |
| | | Single nucleotide variant (3 prime UTR variant) | Early-onset generalized limb-onset dystonia | |
| | | Single nucleotide variant (3 prime UTR variant) | Early-onset generalized limb-onset dystonia | |
| | | Deletion (frameshift variant +1 more) | TOR1A-related condition | |
| | | Single nucleotide variant (synonymous variant) | Dystonic disorder +1 more | |
| | | Single nucleotide variant (synonymous variant) | Dystonic disorder | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Dystonic disorder +1 more | GConflicting classifications of pathogenicity |
| | | Deletion (inframe_deletion) | Dystonia, early-onset atypical, with myoclonic features | |
| | | Single nucleotide variant (missense variant) | Dystonic disorder | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Deletion (frameshift variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Early-onset generalized limb-onset dystonia | |
| | | Single nucleotide variant (missense variant) | Arthrogryposis multiplex congenita 5 | |
| | | Single nucleotide variant (nonsense) | not provided | |
| | | Single nucleotide variant (missense variant) | Dystonic disorder | |
| | | Microsatellite (frameshift variant) | Dystonic disorder | |
| | | Microsatellite (frameshift variant) | Early-onset generalized limb-onset dystonia | |
| | | Single nucleotide variant (missense variant) | Dystonic disorder | |
| | | Single nucleotide variant (synonymous variant) | Dystonic disorder | |
| | | Single nucleotide variant (missense variant) | Arthrogryposis multiplex congenita 5 +1 more | |
| | | Single nucleotide variant (missense variant) | Dystonic disorder | |
| | | Microsatellite (inframe_deletion) | TOR1A-related condition +6 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | TOR1A-related condition | |
| | | Single nucleotide variant (missense variant) | Dystonic disorder | |
| | | Single nucleotide variant (nonsense) | Dystonic disorder | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | Dystonic disorder | |
| | | Single nucleotide variant (missense variant) | Dystonic disorder | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Dystonic disorder +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Arthrogryposis multiplex congenita 5 +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Dystonic disorder | |
| | | Single nucleotide variant (nonsense) | not provided | |
| | | Single nucleotide variant (nonsense) | Arthrogryposis multiplex congenita 5 | |
| | | Single nucleotide variant (missense variant) | Dystonic disorder | |
| | | Single nucleotide variant (missense variant) | Early-onset generalized limb-onset dystonia +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Dystonic disorder | |
| | | Single nucleotide variant (synonymous variant) | Dystonic disorder | |
| | | Single nucleotide variant (synonymous variant) | Dystonic disorder +1 more | |
| | | Single nucleotide variant (missense variant) | Dystonic disorder | |
| | | Single nucleotide variant (missense variant) | Dystonic disorder | |
| | | Single nucleotide variant (missense variant) | Dystonic disorder | |
| | | Single nucleotide variant (missense variant) | Dystonic disorder | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Dystonic disorder | |
| | | Single nucleotide variant (intron variant) | Dystonic disorder | |
| | | Single nucleotide variant (intron variant) | not specified +3 more | |
| | | Deletion (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Duplication (intron variant) | not provided | |
| | | 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) | Dystonic disorder | |
| | | Single nucleotide variant (intron variant) | Early-onset generalized limb-onset dystonia +1 more | |
| | | Single nucleotide variant (splice donor variant) | TOR1A-related condition | |
| | | Single nucleotide variant (missense variant) | Dystonic disorder | |
| | | Single nucleotide variant (missense variant) | Dystonic disorder | |
| | | Single nucleotide variant (synonymous variant) | Dystonic disorder | |
| | | Single nucleotide variant (missense variant) | Dystonic disorder | |
| | | Single nucleotide variant (synonymous variant) | Dystonic disorder | |
| | | Single nucleotide variant (missense variant) | Dystonic disorder +2 more | |
| | | Single nucleotide variant (missense variant) | Dystonic disorder +1 more | |
| | | Single nucleotide variant (synonymous variant) | Dystonic disorder | |
| | | Single nucleotide variant (missense variant) | Early-onset generalized limb-onset dystonia | |
| | | Single nucleotide variant (synonymous variant) | Dystonic disorder | |
| | | Deletion (frameshift variant) | Dystonic disorder | |
| | | Single nucleotide variant (missense variant) | Dystonic disorder | |
| | | Single nucleotide variant (missense variant) | not specified +4 more | |