Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Mendelics | RCV000709046 | SCV000838280 | uncertain significance | Hereditary cancer-predisposing syndrome | 2018-07-02 | criteria provided, single submitter | clinical testing | |
Mendelics | RCV000988010 | SCV001137556 | uncertain significance | Fanconi anemia complementation group U | 2019-05-28 | criteria provided, single submitter | clinical testing |