Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Center for Human Genetics, |
RCV000660131 | SCV000782122 | likely pathogenic | Neurofibromatosis, type 2 | 2016-11-01 | criteria provided, single submitter | clinical testing |