Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000530091 | SCV000629941 | pathogenic | Polyglandular autoimmune syndrome, type 1 | 2017-09-28 | criteria provided, single submitter | clinical testing | A gross deletion of the genomic region encompassing the full coding sequence of the AIRE gene has been identified. The boundaries of this event are unknown as the deletion extends beyond the assayed region for this gene and therefore may encompass additional genes. A whole gene deletion of AIRE has been observed on the opposite chromosome (in trans) from a pathogenic variant in two siblings affected with autoimmune polyendocrinopathy candidiasis ectodermal dystrophy (APECED) (PMID: 18682433). This finding is consistent with autosomal recessive inheritance, and suggests that this deletion contributes to disease. Loss-of-function variants in AIRE are known to be pathogenic (PMID: 11524731, 26141571). For these reasons, this variant has been classified as Pathogenic. |