| | | Single nucleotide variant (missense variant) | Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies | |
| | | Single nucleotide variant (missense variant) | Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies | |
| | | Single nucleotide variant (missense variant) | Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies | |
| | | Single nucleotide variant (nonsense) | Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies | |
| | | Deletion (frameshift variant) | Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies | |
| | | Single nucleotide variant (intron variant) | Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies +1 more | |
| | | Single nucleotide variant (missense variant) | Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies | |
| | | Single nucleotide variant (missense variant) | Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies | |
| | | Microsatellite (frameshift variant) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Microsatellite (5 prime UTR variant +1 more) | Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies | |
| | | Single nucleotide variant (nonsense) | Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies | |
| | | Single nucleotide variant (nonsense) | not provided +1 more | |
| | | Deletion (5 prime UTR variant +1 more) | Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies +1 more | |
| | | Single nucleotide variant (missense variant) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies | |
| | | Single nucleotide variant (missense variant) | Intellectual disability +2 more | |
| | | Single nucleotide variant (splice acceptor variant) | Intellectual disability +2 more | |
| | | Deletion (frameshift variant) | Intellectual disability +2 more | |
| | | Single nucleotide variant (nonsense) | not provided +5 more | |