Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV002525706 | SCV000561768 | likely benign | Dyskeratosis congenita, autosomal dominant 2; Idiopathic Pulmonary Fibrosis | 2024-01-31 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV002393209 | SCV002703309 | likely benign | Dyskeratosis congenita; Hereditary cancer-predisposing syndrome | 2022-03-23 | 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. |
KCCC/NGS Laboratory, |
RCV003316622 | SCV004015600 | likely benign | Acute myeloid leukemia | 2023-07-07 | criteria provided, single submitter | clinical testing |