Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Counsyl | RCV000671630 | SCV000796622 | uncertain significance | Pendred syndrome | 2017-12-20 | criteria provided, single submitter | clinical testing | |
Gene |
RCV002225713 | SCV002504218 | likely benign | not provided | 2020-11-17 | criteria provided, single submitter | clinical testing | See Variant Classification Assertion Criteria. |
Invitae | RCV002225713 | SCV004295496 | benign | not provided | 2023-02-14 | criteria provided, single submitter | clinical testing |