Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000652926 | SCV000774798 | benign | Ullrich congenital muscular dystrophy 2; Bethlem myopathy 2 | 2024-01-26 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001584509 | SCV001819231 | likely benign | not provided | 2021-03-08 | criteria provided, single submitter | clinical testing |