| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | RUNX1, RUNX1-AS1 (R204Q +1 more) | Single nucleotide variant (missense variant) | Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 | |
| | RUNX1, RUNX1-AS1 (E138D +1 more) | Single nucleotide variant (missense variant) | not provided +1 more | |
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