Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000472176 | SCV000563860 | pathogenic | Telangiectasia, hereditary hemorrhagic, type 1 | 2016-10-12 | criteria provided, single submitter | clinical testing | A gross deletion of the genomic region encompassing the full coding sequence of the ENG 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. Loss-of-function variants in ENG are known to be pathogenic (PMID: 15879500). This particular variant has been reported in the literature in individuals with hereditary hemorrhagic telangiectasia syndrome (PMID: 20414677, 24267784). For these reasons, this variant has been classified as Pathogenic. |