Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001494922 | SCV001699588 | likely benign | Werner syndrome | 2023-04-03 | criteria provided, single submitter | clinical testing | |
Genetic Services Laboratory, |
RCV001820198 | SCV002064745 | uncertain significance | not specified | 2020-08-18 | criteria provided, single submitter | clinical testing |