Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000945921 | SCV001091996 | benign | Epileptic encephalopathy | 2023-10-28 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003925857 | SCV004747021 | likely benign | FASN-related condition | 2022-02-24 | 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). |