Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000456287 | SCV000556585 | benign | Tuberous sclerosis 2 | 2023-11-02 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV001016280 | SCV001177218 | likely benign | Hereditary cancer-predisposing syndrome | 2019-06-21 | 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. |
Gene |
RCV001712315 | SCV001940290 | likely benign | not provided | 2018-12-07 | criteria provided, single submitter | clinical testing | This variant is associated with the following publications: (PMID: 23619168) |
Genome- |
RCV000456287 | SCV002039236 | benign | Tuberous sclerosis 2 | 2021-11-07 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003960053 | SCV004767143 | likely benign | TSC2-related condition | 2019-07-10 | criteria provided, single submitter | clinical testing | This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications). |