Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000424096 | SCV000524069 | likely benign | not specified | 2016-03-04 | 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 |
RCV000728096 | SCV000855629 | uncertain significance | not provided | 2017-07-07 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV000728096 | SCV001089489 | likely benign | not provided | 2024-01-20 | criteria provided, single submitter | clinical testing |