Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV000164181 | SCV000214801 | likely benign | Hereditary cancer-predisposing syndrome | 2014-03-31 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000524609 | SCV000629159 | likely benign | Peutz-Jeghers syndrome | 2017-06-17 | criteria provided, single submitter | clinical testing |