Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Women's Health and Genetics/Laboratory Corporation of America, |
RCV000030270 | SCV000052937 | uncertain | Lynch syndrome | 2011-08-18 | criteria provided, single submitter | curation | Converted during submission to Uncertain significance. |
Invitae | RCV001518389 | SCV001727067 | benign | Hereditary nonpolyposis colorectal neoplasms | 2022-12-31 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001588832 | SCV001826747 | likely benign | not provided | 2019-11-09 | criteria provided, single submitter | clinical testing | This variant is associated with the following publications: (PMID: 10786688, 30238922) |
Sema4, |
RCV002256009 | SCV002528052 | benign | Hereditary cancer-predisposing syndrome | 2020-07-28 | criteria provided, single submitter | curation | |
Ce |
RCV001588832 | SCV003916108 | likely benign | not provided | 2023-09-01 | criteria provided, single submitter | clinical testing | MSH6: BP4, BS1 |