Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001951438 | SCV002246701 | pathogenic | Polyglandular autoimmune syndrome, type 1 | 2021-08-01 | criteria provided, single submitter | clinical testing | For these reasons, this variant has been classified as Pathogenic. This variant has not been reported in the literature in individuals affected with AIRE-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change creates a premature translational stop signal (p.Glu171Phefs*203) in the AIRE gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in AIRE are known to be pathogenic (PMID: 11524731, 26141571). |
Revvity Omics, |
RCV001951438 | SCV003830392 | likely pathogenic | Polyglandular autoimmune syndrome, type 1 | 2021-12-23 | criteria provided, single submitter | clinical testing |