| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Microsatellite (inframe_deletion) | Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures | |
| | IRF2BPL, LOC107984638 (D18E) | Single nucleotide variant (missense variant) | Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures | |
Click to view in NCBI Gene