ClinGen Resource
ClinGen is a National Institutes of Health (NIH)-funded resource dedicated to building an authoritative central resource that defines the clinical relevance of genes and variants for use in precision medicine and research.
Обзор рабочей группы ClinGen по низкой пенетрантности/рисковому аллелю
GenomeConnect Webinar: Variant Classification
Overview of the ClinGen Congenital Heart Disease Expert Panels
Defining a Disease Entity for Curation
Webinar: GenomeConnect Overview July 2025
Update on the Gene Curation Coalition Database (GenCC DB)
Variant Curation Documents Update
Overview of OMIM
Update on the Myeloid Malignancy VCEP
GenomeConnect Webinar - How to Read a Genetic Test Report
Variant Curation Q&A
Overview of the Hereditary Cancer Clinical Domain
Overview of the Severe Combined Immune Deficiency (SCID)-Combined Immune Deficiency (CID) EPs
GenomeConnect
Data Access, Protection and Confidentiality (DAPC) Working Group
GCI Updates and Gene Curation Q&A
ClinGen Congenital Myopathies GCEP & VCEP: Overview & Updates
GenomeConnect and NothingPink Lunch and Learn
Navigating the ClinVar Database
Celebration of ClinGen Volunteers 2024
How to Upload a Genetic Testing Report
GenomeConnect Webinar- How to Track a Gene in ClinGen
Overview/Updates on the Actionability Working Group
GenomeConnect and ClinVar Webinar
ClinGen Curation of ClinVar Project
GA4GH Variant Representation Specification (VRS)
Gene Curation SOP v11 and GCI updates
GenomeConnect Feature on ClinGen Website
ClinGen Clinical Genomics Career Panel 2024 - Stepping Stone Opportunities