| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126860802, ZMYND11 (E432K +15 more) | Single nucleotide variant (missense variant +1 more) | Intellectual disability, autosomal dominant 30 +6 more | |
| | LOC126860802, ZMYND11 (P346del +15 more) | Deletion (inframe_deletion +1 more) | Intellectual disability, autosomal dominant 30 | |
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