Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Eurofins Ntd Llc |
RCV000593695 | SCV000708322 | uncertain significance | not provided | 2018-01-12 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000818446 | SCV000959060 | benign | Qualitative or quantitative defects of dysferlin | 2024-01-31 | criteria provided, single submitter | clinical testing | |
Athena Diagnostics | RCV000593695 | SCV001477230 | uncertain significance | not provided | 2020-07-13 | criteria provided, single submitter | clinical testing | |
Revvity Omics, |
RCV000593695 | SCV003829568 | uncertain significance | not provided | 2022-06-15 | criteria provided, single submitter | clinical testing | |
Natera, |
RCV001276719 | SCV001463246 | uncertain significance | Autosomal recessive limb-girdle muscular dystrophy type 2B | 2019-10-28 | no assertion criteria provided | clinical testing |