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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_001754.5(RUNX1):c.484A>G (p.Arg162Gly) | Pathogenic | hereditary thrombocytopenia and hematologic cancer predisposition syndrome | 2024-03-26 | 2.0 | ClinGen Myeloid Malignancy Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 2 | RUNX1 |
| View | NM_001754.4(RUNX1):c.484A>G (p.Arg162Gly) | Likely Pathogenic | hereditary thrombocytopenia and hematologic cancer predisposition syndrome | 2021-01-12 | 1.0 | - | RUNX1 |
Showing 1 to 2 of 2 rows