| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | SYNGAP1, SYNGAP1-AS1 (G946E +1 more) | Single nucleotide variant (missense variant) | Intellectual disability, autosomal dominant 5 | |
| | SYNGAP1, SYNGAP1-AS1 (R967* +1 more) | Single nucleotide variant (nonsense) | not provided +1 more | |
Click to view in NCBI Gene