| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | ARHGEF2, LOC122128443 (N429S +4 more) | Single nucleotide variant (missense variant) | not specified | |
| | ARHGEF2, LOC122128443 (V347M +4 more) | Single nucleotide variant (missense variant) | not specified | |
| | ARHGEF2, LOC122128443 (R339Q +4 more) | Single nucleotide variant (missense variant) | not specified | |
| | ARHGEF2, LOC122128443 (A339T +4 more) | Single nucleotide variant (missense variant) | not specified | |
| | ARHGEF2, LOC122128443 (S318G +4 more) | Single nucleotide variant (missense variant) | not specified | |
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