Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genomic Research Center, |
RCV000626273 | SCV000746926 | uncertain significance | Autosomal recessive nonsyndromic hearing loss 28 | 2017-12-18 | criteria provided, single submitter | clinical testing |