Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000651941 | SCV000773798 | benign | Immunodeficiency, common variable, 10 | 2024-01-06 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003945663 | SCV004762753 | likely benign | NFKB2-related condition | 2019-11-14 | 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). |