Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000542635 | SCV000640176 | benign | Van der Woude syndrome 2 | 2024-01-25 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001595014 | SCV001829551 | benign | not provided | 2021-05-04 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003979981 | SCV004789285 | benign | GRHL3-related disorder | 2019-03-20 | criteria provided, single submitter | clinical testing | This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications). |