Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000607706 | SCV000714001 | likely benign | not specified | 2017-05-04 | 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. |
Invitae | RCV002529368 | SCV003313640 | likely benign | Hereditary sensory neuropathy-deafness-dementia syndrome | 2023-07-25 | criteria provided, single submitter | clinical testing |