Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001457088 | SCV001660884 | likely benign | Autoimmune lymphoproliferative syndrome, type III caused by mutation in PRKCD | 2020-02-19 | criteria provided, single submitter | clinical testing |