Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV003649585 | SCV004389161 | likely benign | Peroxisome biogenesis disorder, complementation group 7 | 2023-04-28 | criteria provided, single submitter | clinical testing |