| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Neuronal ceroid lipofuscinosis +4 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene