Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000652944 | SCV000774816 | benign | Ullrich congenital muscular dystrophy 2; Bethlem myopathy 2 | 2024-01-31 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001548491 | SCV001768410 | likely benign | not provided | 2020-09-17 | criteria provided, single submitter | clinical testing |