Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001768180 | SCV002008624 | likely benign | not provided | 2024-06-26 | criteria provided, single submitter | clinical testing | See Variant Classification Assertion Criteria. |
Breakthrough Genomics, |
RCV001768180 | SCV005215308 | likely benign | not provided | criteria provided, single submitter | not provided |