Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001387913 | SCV001588666 | pathogenic | not provided | 2020-07-22 | criteria provided, single submitter | clinical testing | This variant is an in-frame deletion of the genomic region encompassing exon 21 of the USH2A gene. It preserves the integrity of the reading frame. This variant has not been reported in the literature in individuals with USH2A-related conditions. The region of the USH2A gene that includes exon(s) 21 has been determined to be clinically significant (PMID: 18273898, 27460420). Therefore, deletions that encompass that region are likely to disrupt protein function and cause disease. For these reasons, this variant has been classified as Pathogenic. |