Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Eurofins Ntd Llc |
RCV000591265 | SCV000701707 | uncertain significance | not provided | 2016-10-07 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV000591265 | SCV001018615 | likely benign | not provided | 2025-01-20 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003925767 | SCV004739513 | likely benign | MYCN-related disorder | 2022-04-04 | 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). |