| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (nonsense) | Motor tics +3 more | |
| | | Indel (missense variant) | Intellectual disability +3 more | |
| | KCNN2, LOC101927078 (I637M +2 more) | Single nucleotide variant (missense variant +1 more) | not specified +4 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene