Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000531992 | SCV000656124 | likely benign | Ullrich congenital muscular dystrophy 2; Bethlem myopathy 2 | 2024-01-25 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001553491 | SCV001774371 | likely benign | not provided | 2020-10-16 | criteria provided, single submitter | clinical testing |