Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV000563189 | SCV000675767 | likely benign | Hereditary cancer-predisposing syndrome | 2017-02-16 | 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 | RCV001505995 | SCV001710910 | likely benign | Tuberous sclerosis 2 | 2023-08-03 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001505995 | SCV002039472 | benign | Tuberous sclerosis 2 | 2021-11-07 | criteria provided, single submitter | clinical testing | |
Sema4, |
RCV000563189 | SCV002533539 | likely benign | Hereditary cancer-predisposing syndrome | 2021-11-17 | criteria provided, single submitter | curation |