Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Counsyl | RCV000409642 | SCV000488908 | likely benign | Familial adenomatous polyposis 1 | 2016-07-15 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003970089 | SCV004791216 | likely benign | APC-related condition | 2019-07-15 | 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). |