Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV003781944 | SCV004575473 | likely benign | Hereditary factor IX deficiency disease; Thrombophilia, X-linked, due to factor 9 defect | 2023-12-05 | criteria provided, single submitter | clinical testing |