Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002188698 | SCV002482759 | likely benign | Hyper-IgM syndrome type 2 | 2023-12-01 | criteria provided, single submitter | clinical testing |