Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001919028 | SCV002184634 | benign | Noonan syndrome 9 | 2023-11-30 | criteria provided, single submitter | clinical testing | |
New York Genome Center | RCV001919028 | SCV002548802 | uncertain significance | Noonan syndrome 9 | 2021-08-06 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001919028 | SCV002763068 | uncertain significance | Noonan syndrome 9 | criteria provided, single submitter | clinical testing |