Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000880553 | SCV001023655 | likely benign | not provided | 2024-01-13 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003920514 | SCV004737331 | benign | FBN3-related disorder | 2019-05-23 | 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). |