Clinical Domain Working Groups

The Long QT Syndrome (LQTS) GCEP was formed in 2019, and their initial scope of work included 17 genes thought to be associated with SQTS. The group completed evaluation of these genes in 2020, and their findings are described in Adler et al. 2020 (PMID: 31983240). The Hereditary Cardiovascular Disease GCEP now re-evaluates these curations on a periodic basis, as described in the ClinGen recuration procedure. Inactive date - 12/20/21