| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (nonsense +1 more) | Intellectual disability +2 more | |
| | | Deletion (frameshift variant) | Intellectual disability +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (splice acceptor variant) | Congenital cerebellar hypoplasia | |
Click to view in NCBI Gene