Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genomic Research Center, |
RCV000785105 | SCV000923663 | likely pathogenic | Neuropathy, hereditary sensory and autonomic, type 2A | 2019-01-01 | criteria provided, single submitter | clinical testing |