| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126860802, ZMYND11 (P268S +15 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | LOC126860802, ZMYND11 (T300I +15 more) | Single nucleotide variant (missense variant +1 more) | Intellectual disability, autosomal dominant 30 | |
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