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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_000133.3(F9):c.1009G>C (p.Ala337Pro) | Likely Pathogenic | hemophilia B | 2024-10-01 | 2.0 | ClinGen Coagulation Factor Deficiency Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for F9 Version 1.0.0 | F9 |
| View | NM_000133.3(F9):c.1009G>C (p.Ala337Pro) | Likely Pathogenic | hemophilia B | 2024-08-02 | 1.0 | ClinGen Coagulation Factor Deficiency Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for F8 Version 1.0.0 | F9 |
Showing 1 to 2 of 2 rows