Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000640872 | SCV000762476 | likely benign | X-linked lymphoproliferative disease due to XIAP deficiency | 2024-01-02 | criteria provided, single submitter | clinical testing |