Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000611636 | SCV000718592 | likely benign | not specified | 2017-04-19 | criteria provided, single submitter | clinical testing | This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease. |
Invitae | RCV003767510 | SCV004620648 | likely benign | Ehlers-Danlos syndrome, classic type, 1 | 2024-01-13 | criteria provided, single submitter | clinical testing |