Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Counsyl | RCV000663076 | SCV000786150 | likely benign | Peutz-Jeghers syndrome | 2018-03-08 | criteria provided, single submitter | clinical testing | |
Color Diagnostics, |
RCV000771626 | SCV000904234 | likely benign | Hereditary cancer-predisposing syndrome | 2017-11-21 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001692256 | SCV001906586 | benign | not provided | 2015-03-03 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000663076 | SCV002445130 | likely benign | Peutz-Jeghers syndrome | 2024-01-31 | criteria provided, single submitter | clinical testing |