Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002080764 | SCV002380428 | likely benign | Hyper-IgM syndrome type 1 | 2023-12-11 | criteria provided, single submitter | clinical testing |