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Free Raw DNA Data Analysis | 90+ Genetic Traits

Upload your 23andMe, MyHeritage, AncestryDNA, or FTDNA raw data file and get an instant breakdown of 90+ scientifically-validated traits - longevity, metabolism, fitness, vitamins, and brain function. No subscription. No upload to our servers. Just real insights from data you already paid for.

23andMe
MyHeritage
AncestryDNA
FamilyTreeDNA
LivingDNA

Drag & drop your Raw DNA Data

Supports .csv or .txt files from MyHeritage, 23andMe, Ancestry, etc. Your file is analyzed completely offline in your browser.

How it works

Three simple steps. The whole flow takes less than a minute, and your file never touches our infrastructure.

1

Download your raw data

Log into 23andMe, MyHeritage, or AncestryDNA and download your raw data file (.csv or .txt). It's already yours - included with your kit.

How to download?
23andMe
  1. Profile → Browse Raw Data
  2. Scroll down → 'Download Raw Data'
MyHeritage
  1. DNA → Manage DNA kits
  2. Three-dot menu → 'Download data'
AncestryDNA
  1. DNA Results Summary → Settings
  2. Actions → 'Download Raw DNA Data'
2

Drop the file here

Drag-and-drop into the analyzer above. Processing happens entirely in your browser using JavaScript - nothing is uploaded.

3

Read & save your report

Browse 90+ traits across 6 categories with population context and molecular mechanisms. Save as PDF for your records.

What we analyze: 90+ traits across 6 categories

Each trait is mapped to one or more SNPs (single nucleotide polymorphisms) selected from peer-reviewed GWAS studies. Below is a sample - the full list is revealed after you upload.

23 traits

Longevity & Healthspan

  • •FOXO3 longevity gene
  • •SIRT1 metabolic sensor
  • •Klotho anti-aging hormone
  • •APOE Alzheimer's risk
  • •Heart attack risk (9p21)
  • •Statin-induced muscle pain
16 traits

Diet & Metabolism

  • •Lactose intolerance (LCT)
  • •Caffeine sensitivity (CYP1A2)
  • •Plant Omega-3 conversion (FADS1)
  • •Type 2 diabetes risk (TCF7L2)
  • •Fatty liver disease (PNPLA3)
  • •G6PD deficiency / fava-bean reaction
13 traits

Brain & Sleep

  • •Chronotype - early bird/night owl (CLOCK)
  • •Deep sleep need (ADA)
  • •Empathy & social buffering (OXTR)
  • •Stress response: Worrier vs Warrior (COMT)
  • •Memory performance (BDNF)
12 traits

Fitness & Physical Performance

  • •Strength vs endurance (ADRB2)
  • •VO2 Max response (PPARGC1A)
  • •Tendon injury risk (COL5A1)
  • •Sprint vs endurance fiber type (ACTN3)
  • •Muscle soreness & recovery (TNF-alpha)
12 traits

Vitamins & Micronutrients

  • •MTHFR folate metabolism
  • •Vitamin D transport (GC)
  • •B12 absorption (FUT2)
  • •Iron uptake (TMPRSS6)
  • •Hereditary hemochromatosis (HFE C282Y / H63D)
19 traits

Sensory Traits & Quirks

  • •Misophonia / chewing rage (TENM2)
  • •Motion sickness (MUTYH)
  • •Fear of public speaking (TCF4)
  • •Cilantro tasting like soap (OR6A2)
  • •Photic sneeze reflex (ZEB2)

How we compare to paid alternatives

If you've already paid for a DNA kit, you shouldn't have to pay again to actually read what's in it. Here's how our free tool stacks up against the most popular paid services.

FeatureAevosPrometheaseGenomelinkSequencing.com
PriceFree$12$30/mo$30-50/app
Your file never leaves your device
No account or email required
Curated traits
Population context per gene
Downloadable PDF report
Multi-SNP gene resolution (FOXO3, APOE)partial

Frequently asked questions

Everything people typically ask before uploading their DNA file.

Is it really free? What's the catch?

Yes, completely free with no limits. No trial, no credit card, no forced upsell. Our mission is to democratize access to information about the raw DNA data you've already paid for - we don't see why you should pay another 100€ to a third-party service just to read it. The only way we may monetize in the future is through our premium holistic health app, but that's completely separate from this tool.

Is my DNA data safe? Is it uploaded to servers?

Your DNA data never leaves your device. The entire analysis happens directly in your browser using JavaScript. There's no upload, no server, no database, no logs. You can turn off your Wi-Fi before loading the file and it'll still work. This is technically different from Promethease or almost every other service that requires uploading the file to their servers.

Which files are supported?

We support raw DNA data files from 23andMe, MyHeritage, AncestryDNA, FamilyTreeDNA (FTDNA), LivingDNA, and any other provider that exports a CSV or TXT file with RSID and genotype columns. Also works with zipped files once extracted.

I don't have my DNA data yet. How can I get it?

You first need to buy a DNA test from companies like MyHeritage (often the cheapest, around $40-50 during sales), 23andMe, or AncestryDNA. They will mail a saliva collection kit to your home. Once you send it back and receive your results on their website (usually after 3-4 weeks), you can download your raw data file and upload it here for our advanced health analysis.

How do I download my raw DNA data from 23andMe / MyHeritage / Ancestry?

23andMe: Profile → Browse Raw Data → 'Download Raw Data' (at the bottom) → confirm password.
MyHeritage: Account → DNA → Manage DNA kits → 'Download data' → follow email verification.
AncestryDNA: DNA Settings → 'Download Raw DNA Data' → email verification.
In all cases you'll get a .csv or .txt file (sometimes zipped) - that's what you upload here.

Which traits are analyzed?

Over 90 scientifically-documented traits grouped into 6 categories: Longevity & Healthspan (FOXO3, SIRT1, Klotho, APOE), Diet & Metabolism (lactose intolerance, Omega-3 conversion), Brain & Sleep (CLOCK, memory, stress response), Fitness & Physical Performance (VO2 Max, muscle recovery), Vitamins & Micronutrients (MTHFR, vitamin D), and Sensory Traits & Quirks (misophonia, eye color, bitter taste).

How are you different from Promethease, Genomelink, Sequencing.com, or others?

Three key differences: (1) Real privacy - we don't upload anything, while Promethease and most competitors process data server-side. (2) Free with no paywall - Promethease charges $12, Genomelink shows a preview then charges $30/month, Sequencing.com sells individual apps at $30-50 each. (3) Curated interpretations - instead of giving you thousands of raw, unreadable results (like Promethease does), we pre-select the 90+ most clinically-validated traits with readable explanations.

Are the interpretations reliable?

Every SNP we include is chosen based on published, validated GWAS studies with a clear biological effect. However, this is NOT a medical diagnostic test. Genetics only explains part of each trait - environment, lifestyle, and epigenetics often matter more. For clinical decisions, always consult a medical geneticist or your physician.

What is the Relevance score next to each trait?

Relevance is a 0-10 score indicating how important a genotype result is on its own merits. It combines three intrinsic properties of the variant: (1) effect size reported in the literature, (2) severity / medical importance of the associated trait, and (3) rarity of the genotype. It deliberately does not factor in what you can do about the result - that depends on individual clinical context. Scores 0-2 are baseline / curiosity, 4-6 are notable, 7+ deserve clinical attention. The scoring system is proprietary and numbers are independently derived from primary studies.

Can I save or print the report?

Yes. After the analysis you can click 'Print / Save PDF' and get a professionally-formatted report, saveable as a PDF or printable directly from your browser. No account creation needed.

Will you add more traits in the future?

Yes, constantly. We're working on SNPs for genetic skincare, pharmacological sensitivity (PGx), response to specific exercise types, and food preferences. Subscribe to the newsletter below to be notified when new traits ship.

Get notified about new traits

We're constantly adding new genetic markers. Drop your email and we'll let you know when the next batch ships - no spam, ever.

We never see your DNA - this opt-in is purely for product updates.

Scientific References

Aevos is built on peer-reviewed research. Below is a foundational list of the primary Genome-Wide Association Studies (GWAS) and clinical literature used to map the traits in our database.

  • APOE (Alzheimer's & Longevity): Corder EH, et al. "Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families." Science. 1993. PMID: 8346443
  • FOXO3 (Longevity): Willcox BJ, et al. "FOXO3A genotype is strongly associated with human longevity." PNAS. 2008. PMID: 18765803
  • KL (Klotho Anti-Aging Hormone): Arking DE, et al. "Association of human aging with a functional variant of klotho." PNAS. 2002. PMID: 11790841
  • SIRT1 (Metabolic Sensor): Figarska SM, et al. "SIRT1 polymorphism, long-term survival and glucose tolerance in the general population." PLoS One. 2013. PMID: 23554904
  • CLOCK (Circadian Rhythm): Katzenberg D, et al. "A CLOCK polymorphism associated with human diurnal preference." Sleep. 1998. PMID: 9779516
  • MTHFR (Folate Metabolism): Frosst P, et al. "A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase." Nature Genetics. 1995. PMID: 7647779
  • LCT (Lactose Intolerance): Enattah NS, et al. "Independent introduction of two lactase-persistence alleles into human populations reflects different history of adaptation to milk culture." Am J Hum Genet. 2008. PMID: 18177514
  • FADS1 (Omega-3 Conversion): Schaeffer L, et al. "Common genetic variants of the FADS1 FADS2 gene cluster and their reconstructed haplotypes are associated with the fatty acid composition in phospholipids." Hum Mol Genet. 2006. PMID: 16670158
  • ACTN3 (Muscle Performance): MacArthur DG, et al. "Loss of ACTN3 gene function alters mouse muscle metabolism and shows evidence of positive selection in humans." Nature Genetics. 2007. PMID: 17828264
  • CYP1A2 (Caffeine Metabolism): Sachse C, et al. "Functional significance of a C-->A polymorphism in intron 1 of the cytochrome P450 CYP1A2 gene tested with caffeine." Br J Clin Pharmacol. 1999. PMID: 10233211

Note: This is a non-exhaustive list of foundational studies. The complete mapping logic for all 90+ traits involves hundreds of peer-reviewed papers.

Medical Disclaimer: This tool is for educational and informational purposes only. It does not constitute medical advice, diagnosis, or treatment, and is not a substitute for clinical genetic testing. Furthermore, raw data from commercial direct-to-consumer DNA tests (like 23andMe or MyHeritage) does not undergo the same rigorous validation as clinical-grade medical testing, meaning the underlying genotype calls may occasionally contain errors or be less definitive. Genetic predispositions interact with environment and lifestyle - your phenotype is rarely your destiny. Always consult a qualified medical geneticist or healthcare professional before making decisions based on genetic information.

Quick stats

Traits analyzed
90+
Categories
6
Avg. processing time
< 5s
Samples analysed
8343

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