Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001056589 | SCV001221039 | likely benign | Qualitative or quantitative defects of dysferlin | 2023-12-24 | criteria provided, single submitter | clinical testing | |
Revvity Omics, |
RCV003145310 | SCV003831334 | uncertain significance | not provided | 2020-09-15 | criteria provided, single submitter | clinical testing | |
Natera, |
RCV001272841 | SCV001455233 | uncertain significance | Autosomal recessive limb-girdle muscular dystrophy type 2B | 2020-01-17 | no assertion criteria provided | clinical testing |