Features

Everything Inside Your Health Book

SoDNAscan analyzes 256 curated genetic variants across 10 biological systems to create a comprehensive, evidence-scored health narrative unique to you.

Your Book

200+ Pages of Personalized Genetic Insight

Every SoDNAscan book is a comprehensive, evidence-based health narrative tailored to your unique genome. With up to 20 chapters — scaled to the amount of genetic data you provide — your book spans nutrition, exercise, sleep, supplementation, medical monitoring, and more.

Up to 20 Chapters

Your book scales with the genetic data you provide. The more raw data available, the deeper the analysis — covering everything from nutrition and supplementation to medical monitoring and pharmacogenomics.

Evidence-Based Throughout

Every finding is graded against published research with full citations and confidence scoring, so you know exactly how strong the evidence is behind each recommendation.

Actionable, Not Abstract

Each chapter concludes with specific, prioritized recommendations — from dietary adjustments and supplement protocols to screening schedules and a structured 90-day action plan.

Our Methodology

Evidence-Based, Every Step

We don't just analyze your DNA — we show you exactly how strong the evidence is behind every finding. Here's how our pipeline works.

1

Curated SNP Selection

We start with 256 genetic variants selected from peer-reviewed databases — ClinVar, PharmGKB, GWAS Catalog, and SNPedia. Each SNP is chosen for clinical relevance, not volume. We include only variants where the science supports actionable insights.

2

Genotype Matching

Your raw data is parsed and matched against our reference database. We identify your specific genotype for each SNP, calculate risk allele dosage, and flag any data quality issues. Unreadable positions are excluded, not guessed.

3

Automated Analysis

Our analysis engine generates reports for each biological system, constrained by evidence tiers and clinical guidelines. Significance cannot be overstated — every claim must be grounded in published research.

4

Confidence Scoring

Each finding receives a confidence rating based on study quality, sample size, replication status, and population relevance. You see the evidence tier alongside every recommendation, so you and your healthcare provider can prioritize appropriately.

Three Confidence Tiers — So You Know What to Prioritize

Well-Established

Large-scale studies, meta-analyses, and replicated results across diverse populations. These findings have strong scientific consensus.

Example: MTHFR C677T and folate metabolism — confirmed in 50+ studies across 100,000+ participants

Moderate

Supported by multiple independent studies with consistent findings, but with some limitations in sample size, population diversity, or replication.

Example: COMT Val158Met and stress response — replicated in several cohorts, some population variability

Emerging

Based on preliminary research, smaller studies, or recent discoveries. Promising but requires further validation. We flag these clearly so you know.

Example: FTO rs9939609 and exercise response — initial studies show interaction effects, larger trials needed

Data sources: ClinVar (NCBI) · PharmGKB (Stanford) · GWAS Catalog (EMBL-EBI) · SNPedia · Peer-reviewed journals

Analysis performed under strict evidence-tier constraints. For wellness and informational purposes only.

Our Approach

What Makes SoDNAscan Different

We're building the genomic health tool we wished existed — rigorous, transparent, and actually useful.

Confidence Scoring

Every genetic finding is scored by evidence strength — so you know what's well-established versus emerging research.

Anti-Hype Philosophy

We tell you when evidence is weak or conflicting. No exaggerated claims, no fear-mongering — just honest science.

Evidence Standards

Findings are graded against published research with full citations. We show our work so you can verify every claim.

Comprehensive Narrative

Not a list of traits — a cohesive health story that connects your genetics across all biological systems.

Actionable Plans

Every chapter ends with specific, prioritized recommendations you can actually implement in your daily life.

Analysis with Guardrails

Our analysis is constrained by evidence tiers and clinical guidelines — it can't overstate genetic significance.

Coverage

10 Biological Systems Analyzed

Your book covers every major system in your body — not just isolated traits.

Cardiovascular

Heart & circulation health

Metabolic

Energy & weight management

Inflammation

Immune response & recovery

Neurological

Brain health & cognition

Methylation

Detox & gene expression

Musculoskeletal

Bones, joints & muscles

Dermatological

Skin health & aging

Gut Health

Microbiome & digestion

Hormonal

Endocrine balance

Pharmacogenomics

Drug metabolism & response

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Curated SNPs
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Biological Systems
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Page Books

Built by Researchers, Not Marketers

SoDNAscan is built on curated, peer-reviewed genetic research. Every recommendation is grounded in evidence — not hype. We believe you deserve full transparency about what your DNA can (and can't) tell you.

Compatible with 23andMe Compatible with AncestryDNA

Your genetic data is encrypted, never sold, and deleted upon request. Your privacy is non-negotiable.

Ready to see your genetic insights?

Upload your raw genetic data from 23andMe or AncestryDNA and get your personalized health book.