| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | | Single nucleotide variant (synonymous variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | | Single nucleotide variant (nonsense) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
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