| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | Intellectual disability, X-linked, syndromic, 35 | |
| | | Single nucleotide variant (missense variant +2 more) | Intellectual disability, X-linked, syndromic, 35 +1 more | |
| | | Copy number gain | not provided | |
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