Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Center for Statistical Genetics, |
RCV000754557 | SCV000853295 | pathogenic | Hearing impairment | 2018-10-08 | no assertion criteria provided | research | |
University of Washington Center for Mendelian Genomics, |
RCV000754557 | SCV001439106 | likely pathogenic | Hearing impairment | no assertion criteria provided | research |