Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genome Diagnostics Laboratory, |
RCV001813687 | SCV002060851 | uncertain significance | Noonan syndrome and Noonan-related syndrome | 2019-11-01 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV002074235 | SCV002481528 | likely benign | RASopathy | 2022-09-22 | criteria provided, single submitter | clinical testing |