Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000686084 | SCV000813587 | likely benign | Qualitative or quantitative defects of dysferlin | 2023-10-28 | criteria provided, single submitter | clinical testing | |
Natera, |
RCV001830484 | SCV002082298 | uncertain significance | Autosomal recessive limb-girdle muscular dystrophy type 2B | 2021-08-02 | no assertion criteria provided | clinical testing |