| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Copy number loss | Rett syndrome, congenital variant | |
| | | Deletion (frameshift variant) | FOXG1 disorder | |
| | | Single nucleotide variant (nonsense) | Rett syndrome, congenital variant | |
| | | Deletion (frameshift variant) | Rett syndrome, congenital variant | |
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