| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130009928, SLAIN1 (K151R +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130009928, SLAIN1 (P172L +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene