Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Equipe Genetique des Anomalies du Developpement, |
RCV000677663 | SCV000803803 | likely pathogenic | Autosomal recessive nonsyndromic hearing loss 3 | 2017-08-07 | criteria provided, single submitter | clinical testing |