Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001496288 | SCV001700985 | likely benign | Noonan syndrome 9 | 2023-11-28 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV003243379 | SCV003952895 | likely benign | Inborn genetic diseases | 2023-04-05 | 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. |