Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Mendelics | RCV000987358 | SCV001136637 | likely benign | Cowden syndrome 1 | 2019-05-28 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001712836 | SCV001939737 | benign | not provided | 2020-04-01 | criteria provided, single submitter | clinical testing |