Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Women's Health and Genetics/Laboratory Corporation of America, |
RCV001174922 | SCV001338359 | likely benign | not specified | 2020-02-13 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001485596 | SCV001690034 | likely benign | Noonan syndrome 9 | 2023-10-24 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001485596 | SCV002763111 | likely benign | Noonan syndrome 9 | criteria provided, single submitter | clinical testing |