Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000613777 | SCV000724864 | likely benign | not specified | 2017-11-25 | 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. |
Eurofins Ntd Llc |
RCV000732149 | SCV000860059 | uncertain significance | not provided | 2018-03-06 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000732149 | SCV001062310 | likely benign | not provided | 2023-09-26 | criteria provided, single submitter | clinical testing |