Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002116424 | SCV002446206 | likely benign | Noonan syndrome | 2021-11-01 | criteria provided, single submitter | clinical testing | |
Women's Health and Genetics/Laboratory Corporation of America, |
RCV004700654 | SCV005203326 | likely benign | not specified | 2024-07-08 | criteria provided, single submitter | clinical testing |