Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000547715 | SCV000629009 | likely benign | Noonan syndrome | 2023-06-28 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001755809 | SCV002007004 | likely benign | not provided | 2021-03-28 | criteria provided, single submitter | clinical testing |