| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | KCNN2, LOC101927078 (H657R +2 more) | Single nucleotide variant (missense variant +1 more) | Neurodevelopmental disorder with or without variable movement or behavioral abnormalities | |
| | KCNN2, LOC101927078 (T222A +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Neurodevelopmental disorder with or without variable movement or behavioral abnormalities +2 more | GConflicting classifications of pathogenicity |
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