Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002016991 | SCV002302067 | likely benign | Agammaglobulinemia 3, autosomal recessive | 2022-08-23 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003948871 | SCV004773797 | likely benign | CD79A-related disorder | 2023-10-12 | 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). |