Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Fulgent Genetics, |
RCV000087753 | SCV002813842 | likely pathogenic | Van der Woude syndrome 2 | 2021-11-28 | criteria provided, single submitter | clinical testing | |
OMIM | RCV000087753 | SCV000120647 | pathogenic | Van der Woude syndrome 2 | 2014-01-02 | no assertion criteria provided | literature only |