Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001705003 | SCV000241354 | likely benign | not provided | 2020-10-23 | criteria provided, single submitter | clinical testing | This variant is associated with the following publications: (PMID: 29352316) |
Invitae | RCV000644675 | SCV000766378 | likely benign | Koolen-de Vries syndrome | 2023-07-17 | criteria provided, single submitter | clinical testing |