Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Counsyl | RCV000411496 | SCV000489731 | likely benign | Lynch syndrome 5 | 2016-11-14 | criteria provided, single submitter | clinical testing | |
Color Diagnostics, |
RCV001179950 | SCV001344753 | likely benign | Hereditary cancer-predisposing syndrome | 2019-03-05 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002058856 | SCV002389484 | benign | Hereditary nonpolyposis colorectal neoplasms | 2024-01-28 | criteria provided, single submitter | clinical testing | |
Myriad Genetics, |
RCV000411496 | SCV004018851 | likely benign | Lynch syndrome 5 | 2023-03-27 | criteria provided, single submitter | clinical testing | This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing. |
All of Us Research Program, |
RCV003995914 | SCV004824325 | likely benign | Lynch syndrome | 2023-06-08 | criteria provided, single submitter | clinical testing |