| | 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 (I16M) | Single nucleotide variant (non-coding transcript variant +2 more) | Inborn genetic diseases | |
| | LOC129931299, WARS2 +1 more | Single nucleotide variant (non-coding transcript variant +2 more) | not provided | |
| | LOC129931299, WARS2 +1 more | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | LOC129931299, WARS2 +1 more (I16F) | Single nucleotide variant (non-coding transcript variant +2 more) | Inborn genetic diseases | |
| | LOC129931299, WARS2 +1 more (K8N) | Single nucleotide variant (non-coding transcript variant +2 more) | Inborn genetic diseases | |
| | LOC129931299, WARS2 +1 more (R12C) | Single nucleotide variant (non-coding transcript variant +2 more) | not provided | |
| | LOC129931299, WARS2 +1 more (W13R) | Single nucleotide variant (non-coding transcript variant +2 more) | Inborn genetic diseases +2 more | GConflicting classifications of pathogenicity |
| | LOC129931299, WARS2 +1 more (R7Q) | Single nucleotide variant (5 prime UTR variant +2 more) | not provided | |
| | LOC129931299, WARS2 +1 more (I16T) | Single nucleotide variant (non-coding transcript variant +2 more) | not provided | |
| | LOC129931299, WARS2 +1 more (H4Y) | Single nucleotide variant (non-coding transcript variant +2 more) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | LOC129931299, WARS2 +1 more | Single nucleotide variant (non-coding transcript variant +2 more) | not provided | |
| | LOC129931299, WARS2 +1 more | Single nucleotide variant (non-coding transcript variant +2 more) | not provided | |
| | LOC129931299, WARS2 +1 more | Single nucleotide variant (non-coding transcript variant +2 more) | not provided | |
| | LOC129931299, WARS2 +1 more | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | LOC129931299, WARS2 +1 more | Single nucleotide variant (non-coding transcript variant +2 more) | not provided | |
| | WARS2-AS1, LOC129931299 +1 more (W13G) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases +5 more | GConflicting classifications of pathogenicity |