ClinVar · variants and health
Public archive of genomic variant interpretations and submitted evidence.
Conditions of use
Check the variant, transcript, condition, date, review status and any conflicts between submissions.
Limits and context
NIH does not independently verify all submitted information. Diagnostic use requires review by a genetics professional.
Catalogued source record. Implementation on ELUCENIA and independent scientific review pending.
Relationship with cancer research
Support for research — context required
Archive of variant interpretations for different conditions. Relevance to cancer must be established for each variant, disease and submission, including conflicts.
Applications: Genomics · Biomarkers