Your DNA Already Has the Answers. Most People Never Read Them.

Your supplements, diet, sleep, and medication response may already be written in your genetic data. We turn your raw DNA file into a 200+ page personalized health book, with confidence scores on every finding so you know exactly what to act on.

See What My DNA Reveals
Evidence-Based
256 SNPs Analyzed
Confidence-Scored
Ready in Hours
0
SNPs Analyzed
0
Biological Systems
0+
Pages Per Book
GDPR Compliant
Encrypted & Private
Peer-Reviewed Research
No Trackers
Works with 23andMe Works with AncestryDNA

The Problem

You Are Operating Your Body Without the Manual

Most people spend years guessing: adjusting diet, switching medications, trying supplements, without ever knowing what their biology actually responds to. Your genetic data already contains the answers.

01

You've Tried Everything. Nothing Sticks.

You've cycled through diets. You've stacked supplements. You've overhauled your sleep routine. Some things helped a little. Most didn't. What if the problem isn't your willpower? The interventions may simply have never matched your biology.

02

A Medication That Should Work… Doesn't

Or it works too intensely. Or the side effects hit you harder than anyone else. Medication response is one of the most genetically variable things about you. Yet almost no one checks this before prescribing. Years of trial-and-error may have a genetic explanation.

03

Your Data Exists. It's Just Unreadable.

You took a DNA test. You have the file. But what does rs1801133 actually mean for your cardiovascular risk? What does rs4988235 say about your diet? Right now, that data is sitting unused: a library you can't read.

SoDNAscan turns your raw genetic file into a 200+ page health book that finally explains you, with evidence scores on every finding so you know exactly what to act on.

The Problem With DNA Reports

Why Most DNA Reports Leave You More Confused Than Before

The genetic testing industry has a dirty secret: generating your data is the easy part. Interpreting it meaningfully is where almost everyone fails.

Raw SNP Dumps

A spreadsheet of codes like rs1801133 and rs429358 with no explanation of what they mean, or whether they matter at all.

No Evidence Weighting

Every finding presented at the same confidence level, whether it's backed by a single preliminary study or decades of replicated research.

Isolated Traits

"You may have higher caffeine sensitivity." "You may process saturated fat differently." Disconnected observations with no synthesis across systems.

Zero Actionability

No protocols. No timelines. No prioritization. Knowing a SNP exists is worthless without knowing what to actually do about it.

SoDNAscan was built to solve exactly this.

Every finding is confidence-scored, every system is cross-analyzed, and every insight comes with a specific, prioritized action. Not a data dump. A health book you can actually use.

"I built SoDNAscan because I was tired of genetic health tools that either overpromised or underdelivered. You deserve to know what your DNA can actually tell you, and where the science still has gaps."
Founder, SoDNAscan · Read our story →

Process

How It Works

From raw data to personalized health book in three steps, ready in hours, not weeks.

01

Upload Your Genetic Data

Securely upload your raw DNA file from 23andMe, AncestryDNA, or other major testing services. Your data stays private and encrypted.

You'll finally have somewhere to put that data file you downloaded years ago.

02

256 SNPs Analyzed Across 10 Systems

Your genetic variants are cross-referenced against curated research, with each finding scored by confidence level and evidence strength.

You'll understand which findings are solid science and which are still emerging, so you know exactly what to prioritize.

03

Receive Your Health Book Within Hours

Your 200+ page personalized health book is ready in hours, not weeks. Covering nutrition, supplements, exercise, sleep, medical monitoring, and a 90-day action plan.

You'll know why certain diets, supplements, or medications have worked or haven't, and what to do differently going forward.

The Science

How Our Analysis Works

Rigorous methodology you can verify. Every finding traces back to published research.

256 Curated SNPs

Every variant is hand-selected from peer-reviewed research for clinical relevance and evidence strength. No raw data dumps.

ClinVar, PharmGKB, GWAS Catalog

3-Tier Confidence Scoring

Each finding is rated as Well-Established, Moderate, or Emerging based on study size, replication, and meta-analysis quality. You always know how strong the evidence is.

Based on ClinGen evidence framework

10-System Cross-Analysis

Your genetics don't work in isolation. Our analysis connects findings across cardiovascular, metabolic, neurological, and 7 other systems to surface interactions most reports miss.

Multi-system polygenic modeling

Explore all features and systems →

Pharmacogenomics

Your Genetics Determine How You Process Medications

If a medication never worked for you, or worked too intensely, your genetics may explain why. This is one of the most clinically significant and least-discussed areas in personal health.

The average person tries 2–3 antidepressants before finding one that works. For many, the drug itself is fine. The problem is how their liver processes it. Your SoDNAscan health book includes a full pharmacogenomics chapter covering your metabolizer status across key drug pathways.

Antidepressants & Anxiety

Variants in CYP2D6 and CYP2C19 affect how quickly you metabolize SSRIs and SNRIs. A slow metabolizer may accumulate toxic levels at standard doses; a rapid metabolizer may get no therapeutic effect at all.

ADHD Medications

Stimulant response and tolerance are strongly tied to dopamine pathway genetics (DRD4, COMT). The same dose that gives one person focus may cause anxiety or do nothing for another.

Statins & Heart Medications

SLCO1B1 variants significantly raise the risk of statin-induced muscle damage. Knowing this before starting a statin regimen could prevent years of unexplained pain.

Pain Medications & Opioids

CYP2D6 ultra-rapid metabolizers convert codeine to morphine far too quickly, making a standard dose dangerous. Poor metabolizers on the same dose get no relief at all.

Caffeine & Sleep Aids

CYP1A2 determines how fast you clear caffeine. A slow metabolizer who drinks coffee at 2pm may still have half the caffeine in their system at midnight, directly impacting sleep quality.

Your health book maps your genetic metabolizer status across all major drug pathways, so you and your doctor can make informed decisions rather than guesses.

Get My Pharmacogenomics Report

For informational purposes only. Always consult a qualified healthcare provider before adjusting medications.

Preview

See What Your Book Looks Like

Every SoDNAscan book is a comprehensive, evidence-based health narrative. Here's a preview of the quality you'll receive.

SoDNAscan Health Book
Personalized Genetic Analysis
Chapter 3

Cardiovascular Health

Based on your genetic profile, you carry variants in genes associated with cardiovascular function, including rs1801133 (MTHFR C677T) and rs4961 (ADD1). These findings are contextualized below with confidence ratings.

Well-Established
MTHFR C677T: Homocysteine Metabolism
Your CT genotype is associated with moderately reduced enzyme activity (~35%). Consider monitoring homocysteine levels and ensuring adequate folate intake.
Emerging
ADD1 Gly460Trp: Sodium Sensitivity
Preliminary research suggests your variant may influence blood pressure response to dietary sodium. Current evidence is limited.
Get Your Full Report

Your book includes all 10 biological systems with confidence-scored findings

What Users Say

Real People, Real Insights

See how SoDNAscan helped others understand their genetics.

"I've spent the last three years cycling through diets that my partner thrived on but left me exhausted. After reading my SoDNAscan book, I finally had an explanation: my genetics flag a strong carbohydrate sensitivity and a methylation issue affecting energy metabolism. I stopped guessing and started eating for my actual biology. The difference was immediate."
SM
Sarah M.
23andMe user
"I tried two antidepressants that did nothing, then a third that hit me like a freight train. My psychiatrist had no explanation. My SoDNAscan pharmacogenomics chapter showed I'm a CYP2D6 poor metabolizer. I process certain medications far too slowly at standard doses. I brought the report to my doctor and she changed my prescription approach entirely. I wish I'd had this five years ago."
JT
James T.
AncestryDNA user
"The cardiovascular chapter flagged an elevated clotting risk that I brought to my GP, who ordered follow-up labs I'd never had before. The supplement recommendations are on the premium side and I wish there were more budget alternatives. But the confidence scoring is genuinely different. I could tell which findings were solid science and which to treat as preliminary. That honesty made the whole book more trustworthy."
DK
David K.
23andMe user
We never sell your data
Zero third-party tracking
Delete anytime, no questions
Our full promise →

Pricing

One Book. One Price. Yours Forever.

No subscriptions. No upsells. Pay once and own your personalized health book for life.

Your Personalized Health Book

€200 one-time

Analysis

  • 256 curated SNPs across 10 biological systems
  • 3-tier confidence scoring on every finding
  • Blood work cross-referencing (upload your labs)
  • Wearable data integration (Apple Health, Oura, Fitbit, Whoop)
  • Pharmacogenomics: how you metabolize medications

Your Book

  • 200+ page personalized health book (PDF)
  • Executive summary: your top 10 findings
  • 10 system deep-dives (cardio, metabolic, neuro, immune, and more)
  • Your top 30 foods, chosen for YOUR genetics
  • Phased supplement protocol with dosing and timing
  • Exercise, sleep, and stress playbooks
  • 90-day action plan with weekly milestones
  • Medical monitoring plan with screening schedule
Get Your Health Book

Compatible with 23andMe and AncestryDNA raw data exports. Blood work and wearable data optional but recommended.

For wellness and informational purposes only. Not a medical device.

"I was skeptical about another genetic health service after trying a few that gave me nothing useful. SoDNAscan's report connected findings across 10 systems into an actual health narrative. The confidence scoring really helped me orient myself in the information."
Maria L. — AncestryDNA user

Frequently Asked Questions

How much does a SoDNAscan health book cost?
Our Complete health book is currently available as a one-time purchase. No subscriptions, no hidden fees. Visit our pricing section for current pricing.
Is my genetic data safe?
Your genetic data is encrypted in transit and at rest, never sold to third parties, and deleted upon request. We use only self-hosted, cookie-free analytics with no third-party trackers or advertising pixels. We follow GDPR-compliant data handling protocols.
How long does it take to get my health book?
Once you upload your genetic data, your personalized health book is typically generated in under 30 minutes. You'll receive an email notification when it's ready to view and download.
What raw DNA data do you accept?
We accept raw data files from 23andMe, AncestryDNA, and most other major consumer genetic testing services. You'll download a raw data file from your testing provider and upload it to SoDNAscan.
Is this pseudoscience? How reliable are SNP-based health insights?
The genetic wellness space has a lot of overclaiming, so it's worth asking. We only include SNPs with published research in peer-reviewed journals and established databases (ClinVar, PharmGKB, GWAS Catalog). Each finding is rated Well-Established, Moderate, or Emerging based on study size, replication, and meta-analysis quality. Where evidence is weak or preliminary, we say so explicitly. A finding will never be presented as fact when it's still speculative.
How is SoDNAscan different from Promethease or other raw data tools?
Promethease gives you thousands of raw SNP associations with no filtering, no confidence weighting, and no synthesis. Most users find it overwhelming. SoDNAscan curates 256 clinically relevant SNPs, scores each by evidence strength, cross-analyzes them across 10 biological systems, and delivers a 200+ page book with specific, prioritized action plans. The difference is between a raw database lookup and a structured interpretation.
Why 256 SNPs? Why not analyze everything?
More is not better in genetic health analysis. Most SNPs have no meaningful clinical relevance. Including them inflates the report while diluting actionable signal. Our 256 curated variants were hand-selected from peer-reviewed research for evidence quality, clinical significance, and actionability. Every SNP in our analysis has a specific reason to be there.
View all questions → Decode My DNA

From the Blog

Learn What Your DNA Can Tell You

Evidence-based articles on genetics, raw DNA data, and personalized health.

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