Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV003802828 | SCV004591606 | pathogenic | Asphyxiating thoracic dystrophy 5; Senior-Loken syndrome 8 | 2022-11-24 | criteria provided, single submitter | clinical testing | This variant has not been reported in the literature in individuals affected with WDR19-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change creates a premature translational stop signal (p.Gln623Glufs*10) in the WDR19 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in WDR19 are known to be pathogenic (PMID: 22019273, 23559409, 23683095, 26275793, 27241786, 29068549). For these reasons, this variant has been classified as Pathogenic. |