| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | ARHGEF5, LOC126860212 (N1526D) | Single nucleotide variant (missense variant) | not specified | |
| | ARHGEF5, LOC126860212 (S1512C) | Single nucleotide variant (missense variant) | not specified | |
| | ARHGEF5, LOC126860212 (R1524Q) | Single nucleotide variant (missense variant) | not specified | |
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