Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001511137 | SCV001718328 | benign | not provided | 2024-01-27 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003956136 | SCV004777460 | likely benign | PCLO-related disorder | 2020-01-20 | 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). |