Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV003581333 | SCV004353649 | likely benign | Congenital neutropenia-myelofibrosis-nephromegaly syndrome | 2023-12-16 | criteria provided, single submitter | clinical testing |