Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV002316893 | SCV000850701 | likely benign | Inborn genetic diseases | 2017-05-31 | criteria provided, single submitter | clinical testing | This alteration is classified as likely benign based on a combination of the following: population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity. |
Invitae | RCV001444371 | SCV001647368 | likely benign | Charcot-Marie-Tooth disease axonal type 2O | 2022-03-09 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001585679 | SCV001818748 | likely benign | not provided | 2019-04-08 | criteria provided, single submitter | clinical testing |