Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genetic Services Laboratory, |
RCV001819195 | SCV002067075 | uncertain significance | not specified | 2018-06-05 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV002542548 | SCV003488920 | likely benign | not provided | 2023-12-07 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003892866 | SCV004716721 | likely benign | ANKRD26-related disorder | 2021-11-19 | 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). |