Welcome to ClinVar Miner!

The content on this website is current as of 30 May 2026. On that date, ClinVar had 6,893,173 submissions on 4,519,162 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

Conflict exploration

High-level trends

ClinVar Miner was developed by Alex Henrie at the Eilbeck Lab of the University of Utah Department of Biomedical Informatics with support from the NHGRI's ClinGen Resources (grants U41 HG006834-01A1 to Heidi Rehm and U01 HG007437-01 to Jonathan Berg). Use of NCBI data does not constitute NCBI 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. The submitted information has not been verified. If you have questions about the information contained on this website, please see a health care professional.