Showing 1 to 2 of 2 rows
See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_001754.5(RUNX1):c.1044C>T (p.His348=) | Uncertain Significance | hereditary thrombocytopenia and hematologic cancer predisposition syndrome | 2025-01-15 | 1.1 | - | RUNX1 |
| View | NM_001754.5(RUNX1):c.1044C>T (p.His348=) | Uncertain Significance | hereditary thrombocytopenia and hematologic cancer predisposition syndrome | 2022-07-05 | 1.0 | - | RUNX1 |
Showing 1 to 2 of 2 rows