Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute for Medical Genetics and Human Genetics, |
RCV002287875 | SCV002578169 | uncertain significance | Fanconi anemia complementation group D2 | 2022-09-27 | criteria provided, single submitter | clinical testing |