Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002088482 | SCV002390295 | benign | not provided | 2023-07-03 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003893252 | SCV004717965 | likely benign | OSGEP-related disorder | 2022-12-19 | no assertion criteria provided | 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). |