Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000559817 | SCV000656192 | likely benign | Ullrich congenital muscular dystrophy 2; Bethlem myopathy 2 | 2024-01-22 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001591297 | SCV001825120 | likely benign | not provided | 2021-04-07 | criteria provided, single submitter | clinical testing |