Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute of Human Genetics, |
RCV001843860 | SCV002103043 | uncertain significance | Prader-Willi syndrome | 2021-10-21 | criteria provided, single submitter | clinical testing | PM2 |