Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000795621 | SCV000935089 | benign | Qualitative or quantitative defects of dysferlin | 2023-12-03 | criteria provided, single submitter | clinical testing | |
Natera, |
RCV001830707 | SCV002079861 | uncertain significance | Autosomal recessive limb-girdle muscular dystrophy type 2B | 2020-08-15 | no assertion criteria provided | clinical testing |