Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute of Human Genetics, |
RCV002463409 | SCV002757836 | pathogenic | Coffin-Siris syndrome 12 | 2020-11-02 | criteria provided, single submitter | clinical testing |