Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Center for Human Genetics, |
RCV000659855 | SCV000781734 | pathogenic | X-linked Opitz G/BBB syndrome | 2016-11-01 | criteria provided, single submitter | clinical testing |