Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001478265 | SCV001682533 | likely benign | Qualitative or quantitative defects of dysferlin | 2024-01-18 | criteria provided, single submitter | clinical testing | |
Natera, |
RCV001271541 | SCV001452774 | likely benign | Autosomal recessive limb-girdle muscular dystrophy type 2B | 2020-09-16 | no assertion criteria provided | clinical testing |