Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Mendelics | RCV000708911 | SCV000837993 | uncertain significance | Lynch syndrome | 2018-07-02 | criteria provided, single submitter | clinical testing | |
Mendelics | RCV000987144 | SCV001136367 | uncertain significance | Colorectal cancer, hereditary nonpolyposis, type 2 | 2019-05-28 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001444066 | SCV001647059 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2018-11-06 | criteria provided, single submitter | clinical testing |