Welcome to ClinVar Miner!

The content on this website is current as of 1 October 2024. On that date, ClinVar had 4,666,990 submissions on 3,068,002 variants. When referencing data from this website, please cite the 2018 Human Mutation article "ClinVar Miner: Demonstrating utility of a Web‐based tool for viewing and filtering ClinVar data" .

Data exploration

• Variants by significance
• Variants by gene
• Variants by condition
• Variants by submitter
• Variants by Mondo condition

Conflict exploration

• Variants in conflict by significance
• Variants in conflict by gene
• Variants in conflict by condition
• Variants in conflict by submitter

High-level trends

• Total submissions by method
• Total submissions by country
• Significance terms

ClinVar Miner was developed by Alex Henrie in the Eilbeck Lab with support from the NHGRI's ClinGen Resources (grants U41 HG006834-01A1 to Heidi Rehm and U01 HG007437-01 to Jonathan Berg). Use of the NCBI logo represents use of NCBI data but does not constitute an approval or endorsement of this application. Source code is available on GitHub under the GNU General Public License.

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.