Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ce |
RCV000658642 | SCV000780424 | uncertain significance | not provided | 2018-03-01 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000699356 | SCV000828062 | likely benign | Autosomal dominant Parkinson disease 8 | 2023-05-12 | criteria provided, single submitter | clinical testing | |
Mendelics | RCV000699356 | SCV001138690 | uncertain significance | Autosomal dominant Parkinson disease 8 | 2019-05-28 | criteria provided, single submitter | clinical testing | |
Revvity Omics, |
RCV000658642 | SCV004236278 | uncertain significance | not provided | 2019-11-25 | criteria provided, single submitter | clinical testing |