| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130061165, RSAD1 (R39H) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC130061165, RSAD1 (A13V) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC112533651, RSAD1 (H286P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene