Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001697911 | SCV000724204 | likely benign | not provided | 2019-05-20 | criteria provided, single submitter | clinical testing | |
Invitae | RCV003767633 | SCV001532441 | likely benign | FG syndrome | 2024-01-29 | criteria provided, single submitter | clinical testing |