Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
International Society for Gastrointestinal Hereditary Tumours |
RCV000075012 | SCV000108232 | no known pathogenicity | Lynch syndrome | 2013-09-05 | reviewed by expert panel | research | MAF >1% |
ARUP Laboratories, |
RCV000202203 | SCV001158694 | benign | not specified | 2018-07-02 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001650892 | SCV001865793 | benign | not provided | 2015-03-03 | criteria provided, single submitter | clinical testing | |
Breakthrough Genomics, |
RCV001650892 | SCV005243557 | benign | not provided | criteria provided, single submitter | not provided | ||
Mayo Clinic Laboratories, |
RCV000202203 | SCV000257303 | benign | not specified | no assertion criteria provided | research |