Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001192233 | SCV001360260 | uncertain significance | Hereditary cancer-predisposing syndrome | 2019-01-31 | criteria provided, single submitter | clinical testing | |
Invitae | RCV003619740 | SCV004459281 | likely benign | PTEN hamartoma tumor syndrome | 2023-04-27 | criteria provided, single submitter | clinical testing |