Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001186604 | SCV001353078 | likely benign | Hereditary cancer-predisposing syndrome | 2018-11-06 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001393073 | SCV001594726 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2020-08-22 | criteria provided, single submitter | clinical testing | |
Center for Genomic Medicine, |
RCV003320594 | SCV004024803 | likely benign | not specified | 2023-08-15 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV003996954 | SCV004815884 | likely benign | Lynch syndrome | 2023-02-24 | criteria provided, single submitter | clinical testing |