| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (nonsense +1 more) | Intellectual disability, autosomal dominant 16 | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Intellectual disability, autosomal dominant 16 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | SMARCA4-related BAFopathy +4 more | GConflicting classifications of pathogenicity |
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