Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Eurofins Ntd Llc |
RCV000732948 | SCV000860950 | likely benign | not specified | 2018-04-24 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV000938530 | SCV001084341 | benign | not provided | 2018-07-12 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003965538 | SCV004789419 | likely benign | EHHADH-related disorder | 2022-06-16 | 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). |