Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Department of Genetics, |
RCV003127420 | SCV003803998 | likely pathogenic | O'Donnell-Luria-Rodan syndrome | 2022-10-31 | criteria provided, single submitter | clinical testing |