Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001723539 | SCV001950753 | benign | not provided | 2021-06-19 | criteria provided, single submitter | clinical testing | This variant is associated with the following publications: (PMID: 20427658, 18252210, 30241547) |
OMIM | RCV000005162 | SCV000025339 | uncertain significance | Parkinson disease, late-onset | 2009-02-15 | no assertion criteria provided | literature only |