Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genetic Services Laboratory, |
RCV001820357 | SCV002071132 | uncertain significance | not specified | 2019-08-27 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV004554876 | SCV004731032 | likely benign | BRCA1-related disorder | 2019-07-17 | 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). |