| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | ARHGAP11A-SCG5, SCG5 (R418K +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ARHGAP11A-SCG5, SCG5 (G160V +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | ARHGAP11A-SCG5, SCG5 (P211T +4 more) | Single nucleotide variant (missense variant) | not specified | |
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