Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000547671 | SCV000654800 | likely benign | Immunodeficiency, common variable, 10 | 2023-10-06 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003980018 | SCV004790215 | likely benign | NFKB2-related condition | 2023-11-08 | criteria provided, single submitter | 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). |