Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Prevention |
RCV000242946 | SCV000305347 | benign | not specified | criteria provided, single submitter | clinical testing | ||
Illumina Laboratory Services, |
RCV000394980 | SCV000473330 | benign | Werner syndrome | 2016-06-14 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000836717 | SCV000978563 | likely benign | not provided | 2018-04-09 | 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 | RCV000394980 | SCV001728753 | benign | Werner syndrome | 2024-02-01 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV000394980 | SCV002514978 | benign | Werner syndrome | 2021-12-05 | criteria provided, single submitter | clinical testing |