Variant Pathogenicity Curation
ClinGen variant curation utilizes the 2015 American College of Medical Genetics and Genomics (ACMG) guideline for sequence variant interpretation, which provides an evidence-based framework to classify variants. The results of these analyses will be deposited in ClinVar for community access.
Training Materials
Variant curation training aims to familiarize variant biocurators with general variant assessment information and ClinGen variant curation procedures and resources.
Learn MoreVariant Pathogenicity Curation Interface
The ClinGen Variant Curation Interface is available for public use.
Learn MoreDocuments & Announcements
Documents and announcements related to Variant Pathogenicity Curation.
Learn MoreVariant Curation Results
View detailed evidence supporting the curations of approved ClinGen Variant Curation Expert Panels through the ClinGen Evidence Repository.
Learn MoreFDA Recognition
Variants curated by ClinGen Variant Curation Expert Panels have been recognized by the FDA as a source of valid scientific evidence that can support clinical validity. Click here to learn more about the FDA's recognition of ClinGen as a public human genetic variant database.
Learn MoreClaim Educational Credit for ClinGen Variant Pathogenicity Curations
This module offered through the ACMG Genetics Academy is intended to provide learners with educational credit for participating in ClinGen variant curation activities.
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