Links from Orgtrack
Items: 2
| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion (frameshift variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (missense variant) | Acute myeloid leukemia +2 more | |
Click to view in NCBI Gene