Immune & Inflammation
Autoimmune conditions, inflammation pathways, and immune response markers
GeneGaze turns your raw genetic data into a personal StarMap — scanning 1,100+ clinically significant variants across 10 health categories. No panic. No jargon. Just your constellations.
What is GeneGaze?
Dense lab reports were written for doctors, not for you. GeneGaze reimagines genetic insight — grouping your variants and signals into constellations you can actually navigate. Upload your raw DNA file and get a personal StarMap in minutes.
Every signal gets its weight (clinical priority), its constellation (body system), and its horizon — what it means and what you can actually do next. As educational as possible, by design.
What We Analyze
GeneGaze screens for all clinically significant variants possible — organized into ten mega-groups covering every major system in your body.
Autoimmune conditions, inflammation pathways, and immune response markers
Hereditary cancer susceptibility genes and tumor markers
Cardiovascular health, blood disorders, and clotting factors
Connective tissue conditions, skeletal health, and aging markers
Rare genetic diseases and uncommon variant screening
Pharmacogenomic drug response and enzyme metabolism
Metabolic pathways, nutrient processing, and energy
Neurological conditions, mental health markers, and cognition
Fertility, pregnancy risks, and sex-linked conditions
Hair, eye color, body composition, taste, and sensory predictions — the fun one
Clinically Backed
GeneGaze cross-references every variant against six globally recognized clinical databases — enriched with disease phenotypes, gene function summaries, population frequencies across diverse ancestries, and peer-reviewed literature from Wiley journals.
All variant classifications follow ACMG/AMP 5-tier criteria. ClinVar validation verified March 2026. Disease phenotypes linked via OMIM. Population frequencies from gnomAD v4, TOPMED, and 1000 Genomes. ICD-10/ICD-11 codes for every condition.
What's Inside
1,100+ variants. 50+ medications. Nutrition guidance. Family comparisons. Rare disease screening. All in one app, all on your device.
Your genome organized into 10 constellations covering immune, cancer, cardiac, neurological, metabolic, reproductive, rare disease, medication response, and physical traits.
Pharmacogenomic response profiles for 50+ medications — SSRIs, opioids, statins, blood thinners, and more. Know how your body metabolizes each one before you take it.
Personalized nutrition guidance based on your MTHFR, vitamin metabolism, lactose tolerance, caffeine sensitivity, and more — what to prioritize, what to skip.
Upload up to 3 genome files and compare them side by side — your own from different providers, or your family members'. See exactly where your DNA matches and differs.
All Ehlers-Danlos subtypes, BRCA1/2, Lynch Syndrome, MTHFR, APOE, Wilson's, CF, Tay-Sachs, hemochromatosis, PKU, and 20+ more rare conditions.
Export your full results as a shareable PDF or email them directly — perfect for bringing to a doctor's appointment or a genetic counselor.
Your genome never leaves your device. All analysis runs locally — no cloud upload, no data sharing, no exceptions. Ever.
Results in minutes, not days. Works with 23andMe, AncestryDNA, and other raw DNA files. No lab wait, no subscription — one purchase, yours forever.
Every variant comes with context you can actually understand — what the research says, what the odds mean, and what to discuss with your doctor.
How it works
Privacy by Design
Genetic data is the most personal data that exists. GeneGaze was built from the ground up so your genome stays with you — always.
All analysis runs entirely on your device. No cloud upload, no external servers, no third-party sharing — ever.
No sign-up, no profile, no email collection tied to your data. Your genome is yours and only yours.
Remove your data from the app instantly, with no trace left behind. You're always in control.
Our privacy policy is written in plain language — no legal fog. Read exactly what we do and don't do with your information.
Important Information
GeneGaze gives you unprecedented insight into your own genome — and that power comes with important context to use it wisely.
Consumer genotyping chips (like those from 23andMe and AncestryDNA) can produce false positives at rates around 40% for certain variant types. GeneGaze results are for educational and informational purposes only — they are not a medical diagnosis. Significant findings should always be confirmed with clinical-grade testing through your healthcare provider.
A genetic counselor can help you understand complex findings, decide whether confirmatory testing makes sense, and put your results in the context of your personal and family history. These licensed professionals specialize in exactly this kind of guidance.
Pricing
One-time purchase — no subscription, no recurring fees
Available on iOS. Early access list open now — join before launch.
Early access
GeneGaze is almost ready for launch. Drop your email and you'll be the first to know when it lands on the App Store.
No spam. No data selling. Just your launch notification.
GeneGaze is for educational and informational purposes only. It is not a medical device, does not provide medical advice, and should not be used for making medical decisions without consulting a qualified healthcare provider. Results reflect statistical associations from published research and are not diagnostic. If you have concerns about your health, please speak with a licensed medical professional.