Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001490391 | SCV001694952 | likely benign | Congenital neutropenia-myelofibrosis-nephromegaly syndrome | 2020-08-11 | criteria provided, single submitter | clinical testing |