Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV003868098 | SCV004665534 | likely benign | Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2 | 2023-09-19 | criteria provided, single submitter | clinical testing |