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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_001754.5(RUNX1):c.1086G>T (p.Ser362=) | Benign | hereditary thrombocytopenia and hematologic cancer predisposition syndrome | 2022-07-05 | 1.0 | ClinGen Myeloid Malignancy Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 2 | RUNX1 |
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