Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ce |
RCV001092100 | SCV001248464 | pathogenic | not provided | 2019-11-01 | criteria provided, single submitter | clinical testing | |
University of Washington Center for Mendelian Genomics, |
RCV001291327 | SCV001479800 | likely pathogenic | Hearing loss, autosomal recessive | no assertion criteria provided | research |