Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Center for Statistical Genetics, |
RCV000754556 | SCV000853294 | uncertain significance | Hearing impairment | 2018-10-08 | no assertion criteria provided | research | |
University of Washington Center for Mendelian Genomics, |
RCV000754556 | SCV001439102 | uncertain significance | Hearing impairment | no assertion criteria provided | research |