| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +1 more) | GTP cyclohydrolase I deficiency +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice donor variant) | not provided +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Dystonia 5 +2 more | |
| | | Single nucleotide variant (missense variant) | Dystonia 5 +3 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | |
Click to view in NCBI Gene