Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001392806 | SCV001594455 | likely benign | not provided | 2023-10-17 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003963253 | SCV004785651 | likely benign | CEP250-related disorder | 2020-09-02 | 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). |