Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000559939 | SCV000636985 | benign | Brugada syndrome | 2024-01-22 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001755828 | SCV002006219 | likely benign | not provided | 2018-11-09 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003925636 | SCV004744257 | likely benign | CACNA2D1-related condition | 2024-01-10 | 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). |