Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV005077790 | SCV005716103 | likely benign | Inosine triphosphatase deficiency | 2024-02-10 | criteria provided, single submitter | clinical testing |