See Yourself Differently

See your data
differently

The Haplotype Wallet connects your DNA and health data to your favorite AI. Get clear and simple answers from your AI based on the latest public biobanks, published literature, and models. Stay up to date as science advances. Join the community advancing AI and DNA.

We'll email you when your spot opens up

APOE Status

e3/e4

Reported allele observed

BRCA1

Negative

No pathogenic variants

MTHFR C677T

CT

Heterozygous genotype

Ancestry

78% EUR

4 populations detected

Wellness Score Trend

JanDec

AI Insights

You

You

What can my DNA suggest about my nutrition, weight management, sleep, and fitness?
AI

Claude

Reviewing evidence from thousands of genetic studies on millions of participants....
100K+SNPs analyzed
4Data sources
AIPowered insights
256-bitEncryption

How it works

Three steps from raw file to interoperable biomarker data.

Drop your file here

.txt, .csv, .zip

75%
1

Upload your data

Import files from 23andMe, Ancestry, MyHeritage, or FTDNA. We parse everything automatically.

Parsing genotypes100%
Mapping SNPs100%
Mirroring references87%
Indexing algorithms
2

Connect AI Tools

ChatGPT and Claude can use secure MCP endpoints to combine raw data with the latest algorithms and research databases.

Biomarker traitsOptimal
Metabolic markersOptimal
WellnessOptimal
Variant Lookup4 Regions
3

Explore insights

Use the latest AI to ask educational, research, and wellness questions.

What your wallet can power

Biomarker files hold thousands of data points. We index them for secure access, public reference lookup, and algorithm workflows.

Ancestry composition

See your ethnicity breakdown across global populations with detailed percentages.

Biomarker references

Search mirrored public databases for variant, trait, and study context.

Variant annotations

Look up rsIDs, gene annotations, GWAS entries, and ClinVar records in one place.

Wellness markers

Discover traits for caffeine metabolism, lactose tolerance, vitamin needs, and fitness response.

Import from any major provider

23andMeAncestryMyHeritageFTDNA

Your biomarker data deserves
better than a PDF

We're opening up access in batches. Join the waitlist and we'll email you when it's your turn to turn raw genetic files into a secure, interoperable data workspace.

We'll email you when your spot opens up