| | | Deletion (frameshift variant) | not provided +3 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | not provided +3 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | Syndromic X-linked intellectual disability Lubs type +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Rett syndrome | |
| | | Single nucleotide variant (missense variant) | Rett syndrome | |
| | | Single nucleotide variant (missense variant) | Rett syndrome | |
| | | Single nucleotide variant (nonsense) | Rett syndrome | |
| | | Single nucleotide variant (nonsense) | not provided +8 more | |
| | | Deletion (frameshift variant) | Rett syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Rett syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Rett syndrome | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Syndromic X-linked intellectual disability Lubs type +9 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Rett syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Rett syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Rett syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Autism, susceptibility to, X-linked 3 +7 more | GPathogenic/Likely pathogenic |
| | | Copy number gain | not provided | |
| | | Copy number gain | Syndromic X-linked intellectual disability Lubs type | |