Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV003865130 | SCV004672570 | likely benign | Hyper-IgM syndrome type 2 | 2022-12-14 | criteria provided, single submitter | clinical testing |