Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
International Society for Gastrointestinal Hereditary Tumours |
RCV000074995 | SCV000108213 | no known pathogenicity | Lynch syndrome | 2013-09-05 | reviewed by expert panel | research | MAF >1% |
Counsyl | RCV000412274 | SCV000488266 | benign | Hereditary nonpolyposis colorectal cancer type 5 | 2016-02-10 | criteria provided, single submitter | clinical testing | |
ARUP Laboratories, |
RCV001001447 | SCV001158688 | benign | not specified | 2018-07-02 | criteria provided, single submitter | clinical testing |