| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Intellectual disability | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | ARHGEF6, LOC130068760 (C57R) | Single nucleotide variant (missense variant) | Intellectual disability, X-linked 46 +3 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene