| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Intellectual disability +1 more | |
| | | Single nucleotide variant (missense variant) | Syndromic X-linked intellectual disability Raymond type | GConflicting classifications of pathogenicity |
| | | Duplication (splice acceptor variant) | ZDHHC9-related disorder +1 more | |
Click to view in NCBI Gene