| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | ARHGDIA, LOC130061973 (N69S) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ARHGDIA, LOC130061973 (P68S) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
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