Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000796223 | SCV000935728 | likely benign | Qualitative or quantitative defects of dysferlin | 2023-08-23 | criteria provided, single submitter | clinical testing | |
Mayo Clinic Laboratories, |
RCV001507562 | SCV001713181 | uncertain significance | not provided | 2019-06-03 | criteria provided, single submitter | clinical testing | |
Natera, |
RCV001272837 | SCV001455229 | uncertain significance | Autosomal recessive limb-girdle muscular dystrophy type 2B | 2020-03-17 | no assertion criteria provided | clinical testing |