Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
National Institute on Deafness and Communication Disorders, |
RCV000417149 | SCV000494735 | uncertain significance | Autosomal recessive nonsyndromic hearing loss 3 | 2016-03-01 | no assertion criteria provided | research | |
University of Washington Center for Mendelian Genomics, |
RCV001291112 | SCV001479478 | likely pathogenic | Hearing loss, autosomal recessive | no assertion criteria provided | research |