Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001644097 | SCV001857545 | benign | not provided | 2021-05-12 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001730895 | SCV001981353 | benign | Arthrogryposis multiplex congenita 1, neurogenic, with myelin defect | 2021-08-19 | criteria provided, single submitter | clinical testing |