Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000528907 | SCV000660171 | benign | Congenital disorder of glycosylation, type IIq | 2024-01-28 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001672875 | SCV001888396 | benign | not provided | 2019-04-10 | criteria provided, single submitter | clinical testing |