| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion (frameshift variant) | Intellectual disability, X-linked 99, syndromic, female-restricted | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Intellectual disability, X-linked 99 +2 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene