Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001703861 | SCV000526070 | likely benign | not provided | 2019-06-26 | criteria provided, single submitter | clinical testing | This variant is associated with the following publications: (PMID: 26976419) |
Invitae | RCV000526975 | SCV000624826 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2024-01-03 | criteria provided, single submitter | clinical testing | |
Color Diagnostics, |
RCV000580406 | SCV000685363 | likely benign | Hereditary cancer-predisposing syndrome | 2015-06-01 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV004000420 | SCV004834562 | likely benign | Lynch syndrome | 2024-02-05 | criteria provided, single submitter | clinical testing |