Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002124966 | SCV002405884 | benign | Immunodeficiency, common variable, 10 | 2023-11-29 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003933474 | SCV004753746 | likely benign | NFKB2-related disorder | 2020-01-14 | 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). |