Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000652948 | SCV000774820 | likely benign | Ullrich congenital muscular dystrophy 2; Bethlem myopathy 2 | 2024-01-29 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001559678 | SCV001781961 | likely benign | not provided | 2020-10-14 | criteria provided, single submitter | clinical testing |