Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000839926 | SCV000981837 | likely benign | not provided | 2018-03-13 | 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 | RCV000839926 | SCV002473831 | benign | not provided | 2024-01-08 | criteria provided, single submitter | clinical testing | |
Ce |
RCV000839926 | SCV004159129 | likely benign | not provided | 2022-12-01 | criteria provided, single submitter | clinical testing | ADGRV1: BP4, BP7 |