Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
National Institute on Deafness and Communication Disorders, |
RCV000681546 | SCV000807739 | pathogenic | Autosomal recessive nonsyndromic hearing loss 2 | 2018-07-05 | no assertion criteria provided | research | |
University of Washington Center for Mendelian Genomics, |
RCV001291097 | SCV001479463 | likely pathogenic | Hearing loss, autosomal recessive | no assertion criteria provided | research |