Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Equipe Genetique des Anomalies du Developpement, |
RCV000656441 | SCV000678328 | likely pathogenic | Intellectual disability | 2017-01-01 | criteria provided, single submitter | research |