Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Counsyl | RCV000672722 | SCV000797856 | likely benign | Autosomal recessive limb-girdle muscular dystrophy type 2B | 2018-02-13 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001449061 | SCV001652166 | likely benign | Qualitative or quantitative defects of dysferlin | 2022-12-04 | criteria provided, single submitter | clinical testing |