Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000930220 | SCV001075866 | likely benign | Qualitative or quantitative defects of dysferlin | 2024-01-31 | criteria provided, single submitter | clinical testing | |
Natera, |
RCV001276878 | SCV001463493 | uncertain significance | Autosomal recessive limb-girdle muscular dystrophy type 2B | 2020-01-17 | no assertion criteria provided | clinical testing |