Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000614978 | SCV000714219 | benign | not specified | 2017-12-12 | 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 | RCV000945325 | SCV001091320 | benign | Joubert syndrome 20; Meckel syndrome, type 11 | 2024-01-22 | criteria provided, single submitter | clinical testing |