Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001503835 | SCV001708695 | likely benign | Acute myeloid leukemia | 2021-12-31 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003908794 | SCV004726125 | likely benign | CEBPA-related disorder | 2022-04-27 | 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). |