Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002770913 | SCV003030290 | likely benign | Congenital neutropenia-myelofibrosis-nephromegaly syndrome | 2024-04-17 | criteria provided, single submitter | clinical testing |