Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Department of Molecular and Human Genetics, |
RCV001195148 | SCV001334107 | pathogenic | Autosomal recessive nonsyndromic hearing loss 1B | 2020-04-16 | no assertion criteria provided | clinical testing |