Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000442156 | SCV000512610 | benign | not specified | 2015-07-09 | 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 | RCV000862292 | SCV001002776 | benign | Autosomal dominant nocturnal frontal lobe epilepsy | 2024-01-18 | criteria provided, single submitter | clinical testing | |
Psychiatry Genetics Yale University | RCV000084616 | SCV000116752 | not provided | Tobacco use disorder | no assertion provided | not provided |