Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001223092 | SCV001395225 | likely benign | not provided | 2023-10-24 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001223092 | SCV001992759 | uncertain significance | not provided | 2019-06-20 | criteria provided, single submitter | clinical testing | In silico analysis, which includes protein predictors and evolutionary conservation, supports that this variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge |