Total submissions: 6
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000119218 | SCV000153960 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2024-01-09 | criteria provided, single submitter | clinical testing | |
Color Diagnostics, |
RCV000582091 | SCV000689875 | likely benign | Hereditary cancer-predisposing syndrome | 2017-08-10 | criteria provided, single submitter | clinical testing | |
Counsyl | RCV000663206 | SCV000786389 | likely benign | Colorectal cancer, hereditary nonpolyposis, type 2 | 2018-04-25 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001650975 | SCV001865604 | likely benign | not provided | 2021-04-09 | criteria provided, single submitter | clinical testing | |
Myriad Genetics, |
RCV000663206 | SCV004018153 | likely benign | Colorectal cancer, hereditary nonpolyposis, type 2 | 2023-03-14 | 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, |
RCV003997306 | SCV004831282 | likely benign | Lynch syndrome | 2023-11-20 | criteria provided, single submitter | clinical testing |