| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Platelet-type bleeding disorder 20 | |
| | LOC107985033, SLFN14 (Q452H) | Single nucleotide variant (non-coding transcript variant +1 more) | Platelet-type bleeding disorder 20 | |
| | | Single nucleotide variant (missense variant) | Platelet-type bleeding disorder 20 | |
Click to view in NCBI Gene