Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001722665 | SCV000719036 | likely benign | not provided | 2021-06-07 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002063216 | SCV002356896 | likely benign | Gorlin syndrome | 2024-01-24 | criteria provided, single submitter | clinical testing |