Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000958478 | SCV000730102 | likely benign | not provided | 2019-10-07 | criteria provided, single submitter | clinical testing | This variant is associated with the following publications: (PMID: 10958763) |
Invitae | RCV000958478 | SCV001105325 | likely benign | not provided | 2024-01-25 | criteria provided, single submitter | clinical testing |