Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001651911 | SCV001865297 | benign | not provided | 2021-05-04 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001730905 | SCV001981348 | benign | Arthrogryposis multiplex congenita 1, neurogenic, with myelin defect | 2021-08-19 | criteria provided, single submitter | clinical testing |