| | LOC129931299, WARS2
+1 more (W13R) | Single nucleotide variant (non-coding transcript variant +2 more) | Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures | |
| | LOC129931299, WARS2
+1 more (W13R) | Single nucleotide variant (non-coding transcript variant +2 more) | Inborn genetic diseases +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Parkinsonism-dystonia 3, childhood-onset | |
| | | Single nucleotide variant (missense variant +2 more) | Parkinsonism-dystonia 3, childhood-onset | |
| | | Single nucleotide variant (missense variant) | Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures | |
| | | Single nucleotide variant (missense variant +1 more) | Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures | |
| | LOC129388598, WARS2
+1 more | Deletion (splice acceptor variant +3 more) | Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures | |
| | | Single nucleotide variant (nonsense +1 more) | Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures | |
| | | Single nucleotide variant (missense variant +2 more) | Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures | |
| | | Single nucleotide variant (missense variant) | Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures | |
| | | Deletion (frameshift variant +1 more) | Inborn genetic diseases +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures +3 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (inframe_deletion +1 more) | Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures +1 more | GConflicting classifications of pathogenicity |
| | LOC129931299, WARS2
+1 more (W13G) | Single nucleotide variant (missense variant +2 more) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant +1 more) | not provided | |