Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Counsyl | RCV000662732 | SCV000785501 | likely benign | Familial adenomatous polyposis 1 | 2017-08-22 | criteria provided, single submitter | clinical testing | |
Myriad Genetics, |
RCV003316783 | SCV004020034 | benign | Familial adenomatous polyposis 1 | 2023-02-13 | criteria provided, single submitter | clinical testing | This variant is considered benign. This variant is intronic and is not expected to impact mRNA splicing. |