Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000877902 | SCV001020713 | likely benign | Treacher Collins syndrome 1 | 2023-11-13 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001692315 | SCV001908695 | benign | not provided | 2020-03-18 | criteria provided, single submitter | clinical testing | This variant is associated with the following publications: (PMID: 33206719) |