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See Report
Preferred Variant Title
Classification
Condition
Published Date
Version
Criteria Specification
Gene
View NM_001754.5(RUNX1):c.648C>G (p.Pro216=)
Likely Benign
hereditary thrombocytopenia and hematologic cancer predisposition syndrome2024-09-18
1.0
ClinGen Myeloid Malignancy Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 2RUNX1
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