Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001438771 | SCV001641651 | likely benign | Congenital disorder of deglycosylation | 2023-12-09 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001553269 | SCV001774109 | likely benign | not provided | 2021-03-22 | criteria provided, single submitter | clinical testing |