Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute of Human Genetics, |
RCV001253461 | SCV001429175 | pathogenic | Hyper-IgM syndrome type 1 | 2017-01-01 | criteria provided, single submitter | clinical testing |