Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001187643 | SCV001354497 | likely benign | Hereditary cancer-predisposing syndrome | 2023-05-24 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002057038 | SCV002346947 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2023-10-28 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV003997047 | SCV004830257 | likely benign | Lynch syndrome | 2023-06-08 | criteria provided, single submitter | clinical testing | |
Mayo Clinic Laboratories, |
RCV000202245 | SCV000257269 | uncertain significance | not specified | no assertion criteria provided | research |