Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Counsyl | RCV000662420 | SCV000784858 | uncertain significance | Colorectal cancer, hereditary nonpolyposis, type 2 | 2017-01-19 | criteria provided, single submitter | clinical testing | |
Women's Health and Genetics/Laboratory Corporation of America, |
RCV000030232 | SCV000052899 | uncertain significance | Lynch syndrome | 2015-10-02 | no assertion criteria provided | clinical testing |