Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000554512 | SCV000649716 | likely benign | Qualitative or quantitative defects of dysferlin | 2023-10-29 | criteria provided, single submitter | clinical testing | |
Mayo Clinic Laboratories, |
RCV001508442 | SCV001714591 | uncertain significance | not provided | 2019-07-22 | criteria provided, single submitter | clinical testing | |
Natera, |
RCV001834796 | SCV002082359 | uncertain significance | Autosomal recessive limb-girdle muscular dystrophy type 2B | 2020-12-07 | no assertion criteria provided | clinical testing |