| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (missense variant) | Poirier-Bienvenu neurodevelopmental syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Duplication (frameshift variant) | CSNK2B-related intellectual disability with or without epilepsy | |
Click to view in NCBI Gene