Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000965772 | SCV001113049 | benign | not provided | 2018-12-28 | criteria provided, single submitter | clinical testing | |
Breakthrough Genomics, |
RCV000965772 | SCV005271828 | benign | not provided | criteria provided, single submitter | not provided | ||
Prevention |
RCV003916196 | SCV004731054 | likely benign | TEX15-related disorder | 2019-02-25 | 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). |