Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genomic Research Center, |
RCV000791019 | SCV000930285 | likely pathogenic | Neuropathy, hereditary sensory, type 1D | 2019-04-27 | criteria provided, single submitter | clinical testing |