Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001045478 | SCV001209331 | likely benign | Ullrich congenital muscular dystrophy 2; Bethlem myopathy 2 | 2022-12-02 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV001045478 | SCV002787538 | uncertain significance | Ullrich congenital muscular dystrophy 2; Bethlem myopathy 2 | 2022-01-28 | criteria provided, single submitter | clinical testing |