Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002108663 | SCV002432707 | likely benign | Autosomal dominant Parkinson disease 8 | 2024-01-24 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV002337329 | SCV002638974 | likely benign | Inborn genetic diseases | 2022-02-24 | criteria provided, single submitter | clinical testing | This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, 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. |
Fulgent Genetics, |
RCV002108663 | SCV002806263 | likely benign | Autosomal dominant Parkinson disease 8 | 2021-10-07 | criteria provided, single submitter | clinical testing |