Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV003537049 | SCV000647344 | benign | Familial adenomatous polyposis 1 | 2024-01-27 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003900201 | SCV004717529 | likely benign | APC-related condition | 2022-10-24 | criteria provided, single submitter | clinical testing | This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications). |