Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000630452 | SCV000751408 | benign | Common variable immunodeficiency | 2024-01-25 | criteria provided, single submitter | clinical testing | |
ARUP Laboratories, |
RCV002227191 | SCV002506220 | likely benign | not provided | 2022-02-08 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003935748 | SCV004749914 | likely benign | TNFSF12-related disorder | 2019-07-01 | 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). |