Total submissions: 6
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Prevention |
RCV000242907 | SCV000308324 | benign | not specified | criteria provided, single submitter | clinical testing | ||
Gene |
RCV000242907 | SCV000524318 | benign | not specified | 2016-10-11 | 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. |
Athena Diagnostics | RCV000710920 | SCV000841230 | benign | not provided | 2018-08-10 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV000710920 | SCV001722271 | benign | not provided | 2024-01-31 | criteria provided, single submitter | clinical testing | |
Laboratory of Diagnostic Genome Analysis, |
RCV000710920 | SCV001800795 | likely benign | not provided | no assertion criteria provided | clinical testing | ||
Genome Diagnostics Laboratory, |
RCV000242907 | SCV001808509 | benign | not specified | no assertion criteria provided | clinical testing |