Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Neuro |
RCV000585868 | SCV000693824 | likely pathogenic | Lissencephaly due to LIS1 mutation | 2018-01-01 | criteria provided, single submitter | clinical testing |