| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | SYNGAP1, SYNGAP1-AS1 (D900V +1 more) | Single nucleotide variant (missense variant) | Intellectual disability, autosomal dominant 5 | |
| | SYNGAP1, SYNGAP1-AS1 (A1080T +1 more) | Single nucleotide variant (missense variant) | Intellectual disability, autosomal dominant 5 | GConflicting classifications of pathogenicity |
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