Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001032171 | SCV001195478 | pathogenic | Naxos disease; Arrhythmogenic right ventricular dysplasia 12 | 2022-08-22 | criteria provided, single submitter | clinical testing | This variant is a gross deletion of the genomic region encompassing exon(s) 2 of the JUP gene, which includes the initiator codon. This deletion extends beyond the assayed region for this gene and therefore may encompass additional genes. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in JUP are known to be pathogenic (PMID: 10902626). This variant has not been reported in the literature in individuals affected with JUP-related conditions. For these reasons, this variant has been classified as Pathogenic. |