| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | SYNGAP1, SYNGAP1-AS1 (K642T) | Single nucleotide variant (missense variant) | Intellectual disability, autosomal dominant 5 | |
| | SYNGAP1, SYNGAP1-AS1 (V846fs +1 more) | Microsatellite (frameshift variant) | Intellectual disability, autosomal dominant 5 | |
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