Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genetic Services Laboratory, |
RCV000502621 | SCV000594146 | likely benign | not specified | 2016-06-02 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV000933263 | SCV001078957 | benign | not provided | 2018-07-13 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003925454 | SCV004746954 | likely benign | CLIP1-related disorder | 2019-10-28 | 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). |