Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000581719 | SCV000687184 | likely benign | Hereditary cancer-predisposing syndrome | 2017-03-28 | criteria provided, single submitter | clinical testing | |
Preventiongenetics, |
RCV000679095 | SCV000805485 | likely benign | not provided | 2017-04-17 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000679095 | SCV001910769 | benign | not provided | 2015-05-12 | criteria provided, single submitter | clinical testing | This variant is associated with the following publications: (PMID: 23159591) |
Invitae | RCV003538387 | SCV002422503 | benign | Familial adenomatous polyposis 1 | 2024-01-29 | criteria provided, single submitter | clinical testing |