ClinGen considers the sharing of variant interpretations essential for supporting genomic medicine and a critical part of quality assurance for accurate genetic and genomic testing. Open and transparent sharing allows peer-review and knowledge dissemination to ensure the highest quality care of patients.
To apply for status, or to update your status, patient registries can apply here.
Questions about the criteria? Contact firstname.lastname@example.org.
|Patient Registry||Meets requirements||Additional Achievements|
Submitted >100 variants
|>75% from past 5 years1||Classification updates to participants2||Participant matching mechanism3|
Some requirements and additional achievements based on self-reported data by laboratory
* Most recent submission pending ClinVar processing
1 >75% of classified sequence and/or copy number variants from past 5 years submitted
2 Actively provides participants with the option to receive information from the registry about potenital updates to their varaint classifications at the reporting laboratory
3 Registry provides participants with the ability to match with others based on genetic information (gene or variant)