Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genomic Medicine Lab, |
RCV001007882 | SCV001167586 | uncertain significance | Autosomal recessive nonsyndromic hearing loss 21 | 2018-04-19 | criteria provided, single submitter | clinical testing |