Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001486613 | SCV001691073 | likely benign | Noonan syndrome | 2023-11-01 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001773755 | SCV002004729 | likely benign | not provided | 2020-02-21 | criteria provided, single submitter | clinical testing |