Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000950315 | SCV001096612 | likely benign | Cohen syndrome | 2024-01-31 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003960610 | SCV004774927 | likely benign | VPS13B-related disorder | 2021-07-21 | 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). |
Natera, |
RCV000950315 | SCV001454805 | likely benign | Cohen syndrome | 2020-09-16 | no assertion criteria provided | clinical testing |