Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute of Human Genetics, |
RCV001420169 | SCV001622590 | likely pathogenic | O'Donnell-Luria-Rodan syndrome | 2021-04-28 | criteria provided, single submitter | clinical testing |