Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001416605 | SCV001618788 | likely benign | Immunodeficiency, common variable, 10 | 2022-08-31 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003895501 | SCV004709290 | likely benign | NFKB2-related disorder | 2022-09-09 | 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). |