| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +2 more) | Intellectual disability, autosomal dominant 30 | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | LOC126860802, ZMYND11 (S325R +15 more) | Single nucleotide variant (missense variant +1 more) | Intellectual disability, autosomal dominant 30 | |
| | LOC126860802, ZMYND11 (T346fs +15 more) | Deletion (frameshift variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Intellectual disability, autosomal dominant 30 | |
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