Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002627600 | SCV002971991 | likely benign | HNSHA due to aldolase A deficiency | 2022-03-02 | criteria provided, single submitter | clinical testing |