| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +3 more | |
| | | Single nucleotide variant (intron variant) | SYNGAP1-related condition +2 more | |
| | | Single nucleotide variant (synonymous variant) | SYNGAP1-related condition +4 more | |
| | | Single nucleotide variant (synonymous variant) | Intellectual disability, autosomal dominant 5 +4 more | |
| | SYNGAP1, SYNGAP1-AS1 (A1045G +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | |
| | SYNGAP1, SYNGAP1-AS1 (I1115T +1 more) | Single nucleotide variant (missense variant) | SYNGAP1-related condition +4 more | |
| | SYNGAP1, SYNGAP1-AS1 (R1221Q +1 more) | Single nucleotide variant (missense variant) | not specified +1 more | GConflicting classifications of pathogenicity |
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