Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genetic Services Laboratory, |
RCV000193675 | SCV000248304 | benign | not specified | 2016-02-18 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003937702 | SCV004763571 | likely benign | NRXN2-related disorder | 2022-04-11 | 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). |