| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | TBL1XR1, TBL1XR1-AS1 (A197G +1 more) | Single nucleotide variant (missense variant) | Neurodevelopmental disorder | |
| | | Copy number loss | Intellectual disability, autosomal dominant 41 +1 more | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
Click to view in NCBI Gene