Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001304762 | SCV001494057 | likely benign | Qualitative or quantitative defects of dysferlin | 2023-12-17 | criteria provided, single submitter | clinical testing | |
Natera, |
RCV001835471 | SCV002082316 | uncertain significance | Autosomal recessive limb-girdle muscular dystrophy type 2B | 2020-05-06 | no assertion criteria provided | clinical testing |