Links from MedGen
Items: 4
| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Movement disorder +3 more | |
| | | Translocation | Slurred speech | |
| | | Duplication (frameshift variant) | Autosomal recessive ataxia due to ubiquinone deficiency | |
| | | Duplication (frameshift variant) | not provided +1 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene