| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC107985033, SLFN14 (I461K) | Single nucleotide variant (non-coding transcript variant +1 more) | Platelet-type bleeding disorder 20 | |
| | LOC107985033, SLFN14 (A370T) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (nonsense) | Platelet-type bleeding disorder 20 | |
Click to view in NCBI Gene