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Cumulative P/LP Submissions

Pathogenic and Likely Pathogenic variant submissions to ClinVar over time

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Dashboard Methods FAQ

Data Sources

NCBI ClinVar Orphanet (Prevalence) ClinicalTrials.gov

Company

Probably Genetic LinkedIn

© 2026 Probably Genetic Inc.

This dashboard aggregates publicly available data from NCBI ClinVar and other sources to provide insights into genetic disease patient identification trends. Submission counts represent approximate lower bounds and should not be used as precise epidemiological measures. See the Methods page for full methodology and caveats.

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