| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Syndromic X-linked intellectual disability Raymond type +1 more | |
| | | Single nucleotide variant (splice donor variant) | Intellectual disability | |
| | | Single nucleotide variant (missense variant) | Syndromic X-linked intellectual disability Raymond type +2 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene