Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002158253 | SCV002422961 | likely benign | Familial hemophagocytic lymphohistiocytosis 3 | 2023-12-24 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003951152 | SCV004761359 | likely benign | UNC13D-related disorder | 2019-04-03 | 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). |