Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000877505 | SCV001020250 | likely benign | Ullrich congenital muscular dystrophy 2; Bethlem myopathy 2 | 2023-11-13 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001548281 | SCV001768163 | likely benign | not provided | 2021-03-23 | criteria provided, single submitter | clinical testing |