| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Duplication (nonsense) | Syndromic X-linked intellectual disability Raymond type | |
| | | Single nucleotide variant (missense variant) | Syndromic X-linked intellectual disability Raymond type +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Syndromic X-linked intellectual disability Raymond type | |
Click to view in NCBI Gene