| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | ARHGDIA, LOC130061974 (S62F) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | ARHGDIA, LOC130061974 (A60G) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ARHGDIA, LOC130061974 (K43R) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ARHGDIA, LOC130061974 (Q36R) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ARHGDIA, LOC130061974 (S24L) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
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