Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
International Society for Gastrointestinal Hereditary Tumours |
RCV000075913 | SCV000106933 | likely benign | Lynch syndrome | 2013-09-05 | reviewed by expert panel | research | Intronic substitution with no effect on splicing & MAF 0.01-1% |
Mayo Clinic Genetic Testing Laboratories, |
RCV000202112 | SCV000257119 | likely benign | not specified | no assertion criteria provided | clinical testing | ||
University of Washington Department of Laboratory Medicine, |
RCV000209228 | SCV000265258 | likely benign | Hereditary cancer-predisposing syndrome | 2015-12-01 | no assertion criteria provided | clinical testing |