| Submitter |
RCV |
SCV |
Clinical significance |
Condition |
Last evaluated |
Review status |
Method |
Comment |
| Inherited Neuropathy Consortium |
RCV000790167 |
SCV000929558 |
uncertain significance |
Dejerine-Sottas disease |
|
no assertion criteria provided |
literature only |
|
| Genesis Genome Database |
RCV000857021 |
SCV000999591 |
uncertain significance |
Charcot-Marie-Tooth disease |
2019-08-14 |
no assertion criteria provided |
research |
|
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