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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_001754.4(RUNX1):c.985G>A (p.Ala329Thr) | Likely Benign | hereditary thrombocytopenia and hematologic cancer predisposition syndrome | 2020-06-02 | 1.0 | - | RUNX1 |
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