Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001697950 | SCV000722887 | likely benign | not provided | 2020-06-01 | criteria provided, single submitter | clinical testing | |
Invitae | RCV003596061 | SCV001625852 | likely benign | FG syndrome | 2022-11-24 | criteria provided, single submitter | clinical testing |