We believe everyone deserves to understand their genetic blueprint. GenomeInsight brings professional-grade genome analysis to your browser — no lab coat required, no data compromise.
Everything happens in your browser. Your DNA data never touches our servers.
Drop your raw DNA file from 23andMe, AncestryDNA, or any VCF-format file. We support all major consumer testing formats.
Your genome is parsed and analyzed entirely in your browser using JavaScript. No data is ever transmitted to any server.
We compare your SNPs against curated databases of clinically significant variants — health risks, pharmacogenomics, carrier status, and traits.
Receive an interactive, comprehensive report with risk scores, drug interactions, ancestry breakdown, and actionable wellness insights.
We engineered GenomeInsight so that we cannot access your data — even if we wanted to.
We literally cannot see your DNA data. All analysis runs in your browser — no server-side processing, no cloud storage, no exceptions.
Your genetic data never leaves your device. We don't have servers that store DNA. Results are saved only in your browser's local storage.
We don't track which variants you carry or build profiles from your genetic data. Your genome is yours alone.
We support the Genetic Information Nondiscrimination Act. Your genetic data should never be used against you by employers or insurers.
Our analysis is grounded in peer-reviewed research and authoritative genomic databases.
The NHGRI-EBI Catalog of Genome-Wide Association Studies — the gold standard for SNP-trait associations with thousands of published studies.
NCBI's public archive of clinically relevant genomic variants with expert-curated pathogenicity assessments.
The Pharmacogenomics Knowledge Base — curating how genetic variation affects drug response for precision medicine.
Clinical Pharmacogenetics Implementation Consortium provides peer-reviewed, evidence-based gene-drug interaction guidelines.
Health information deserves higher standards than ordinary web content. Here are ours.
Every health claim on this site is grounded in peer-reviewed research, CPIC clinical guidelines, or authoritative public databases (ClinVar, GWAS Catalog, PharmGKB). We do not cite secondary blogs or unsourced claims.
Every reference we publish is checked to resolve to a real publication (DOI-verified against Crossref). If a citation cannot be verified, it does not appear on the site.
Genetics moves fast and we are not infallible. If you spot an error — a miscited study, an outdated claim, a wrong effect size — email contact@genomeinsight.org and we will investigate and correct it promptly.
We sell analysis software, nothing else. No supplements, no lab tests, no affiliate commissions on health products, no sponsored content. Our only incentive is an accurate product.
Our content is educational. It is written to help you understand the published science, not to diagnose, treat, or replace a conversation with a qualified healthcare provider or genetic counselor.
No. GenomeInsight is for educational and informational purposes only. It does not diagnose conditions. Always consult qualified healthcare professionals before making medical decisions based on genetic information.
We support raw data files from 23andMe, AncestryDNA, MyHeritage, FamilyTreeDNA, and any standard VCF-format file. Most consumer testing services let you download your raw data.
Our variant analysis is based on peer-reviewed studies from the GWAS Catalog and ClinVar. However, consumer genotyping chips only test a subset of known variants — clinical-grade sequencing is always more comprehensive.
Since we never store your data on any server, there's nothing to delete on our end. Your results are stored only in your browser's local storage, which you can clear anytime from Settings.
Questions, feedback, or partnership inquiries? We'd love to hear from you.
contact@genomeinsight.org