Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000873816 | SCV001015886 | likely benign | Noonan syndrome | 2024-01-31 | criteria provided, single submitter | clinical testing | |
Women's Health and Genetics/Laboratory Corporation of America, |
RCV002265907 | SCV002548407 | benign | not specified | 2022-05-07 | criteria provided, single submitter | clinical testing |