| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | RUNX1, RUNX1-AS1 (V128I +1 more) | Single nucleotide variant (missense variant) | Acute myeloid leukemia +1 more | |
| | RUNX1, RUNX1-AS1 (A149T +1 more) | Single nucleotide variant (missense variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | RUNX1, RUNX1-AS1 (T121I +1 more) | Single nucleotide variant (missense variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | RUNX1, RUNX1-AS1 (S114* +1 more) | Single nucleotide variant (nonsense) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 +1 more | GPathogenic/Likely pathogenic |
| | RUNX1, RUNX1-AS1 (S141A +1 more) | Single nucleotide variant (missense variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | RUNX1, RUNX1-AS1 (V103I +1 more) | Single nucleotide variant (missense variant) | Hereditary thrombocytopenia and hematologic cancer predisposition syndrome | |
| | RUNX1, RUNX1-AS1 (T101S +1 more) | Single nucleotide variant (missense variant) | Acute myeloid leukemia | |
| | RUNX1, RUNX1-AS1 (D123H +1 more) | Single nucleotide variant (missense variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
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