Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV003002158 | SCV003293268 | likely benign | HNSHA due to aldolase A deficiency | 2022-01-13 | criteria provided, single submitter | clinical testing |