Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001710861 | SCV001938507 | benign | not provided | 2020-09-16 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003956335 | SCV004775892 | likely benign | CTNND2-related disorder | 2024-01-08 | no assertion criteria provided | 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). |