Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000469387 | SCV000559243 | likely benign | Xeroderma pigmentosum, group F; Cockayne syndrome; Fanconi anemia complementation group Q | 2023-02-23 | criteria provided, single submitter | clinical testing | |
Genetic Services Laboratory, |
RCV001821353 | SCV002066730 | likely benign | not specified | 2020-12-08 | criteria provided, single submitter | clinical testing |