for Data Owners

Find out what your genome says about your health — in 30 seconds.

Have a 23andMe or Ancestry file sitting unused? Ask questions in plain language and get instant answers based on your actual DNA. Turn your raw data file into an active health tool you use every day.

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What you get

Get answers faster than Google search

Ask 'What does my genome say about caffeine?' and get your personal answer in 3-5 seconds — not generic population statistics, but YOUR specific variants explained clearly.

New longevity study published today? Check in 60 seconds

Check if you have the variant while your friends are still reading headlines. Your genome already has the answer — no waiting 3-6 months for 23andMe report updates.

Ready data for conversations with your doctor

Get printable tables with citations and references. Walk into appointments prepared with your genetic information formatted professionally.

Your data stays private and secure

Your data is encrypted from the moment you upload it until you view results — no one in between, not even us, can read it. Protected with the same multi-layer encryption banks use for financial transactions. Delete anytime with one click.

Join 1,200+ people who turned their 23andMe data into daily health insights

Real questions from people like you, and the results they got:

→ 'I found out I metabolize caffeine slowly — switched to morning-only coffee and my sleep improved dramatically' — Sarah M.
→ 'Discovered my vitamin D receptor variant. Changed supplementation dose with my doctor. Game changer.' — David K.
→ 'Checked that viral longevity study in 60 seconds. Turns out I have the variant. Sharing with my family now.' — Emily R.
→ 'Finally understand why dairy bothers me. Lactase gene explained everything. Switched to lactose-free and feel amazing.' — Michael T.

See what you'll actually get: Example conversation

You: What does my genome say about caffeine? Ask My DNA: Your CYP1A2 gene (rs762551) shows you're a slow caffeine metabolizer. What this means: ✓ Caffeine stays in your system 2-3x longer than average ✓ Coffee after 2pm may disrupt your sleep ✓ Recommended max: 200mg/day (about 2 cups) Why you can trust this: • Your genotype: A/a at rs762551 • Research: [PMID: 16522833] 'Caffeine metabolism and sleep...' • Population frequency: ~40% have this variant Want to know more? Ask follow-up questions or export this for your doctor.

Ask questions like talking to a geneticist

No medical jargon needed. Just ask naturally and get clear answers with scientific backing.

→ 'What does my APOE gene variant mean for my brain health?'
→ 'Does that new coffee metabolism study apply to me?'
→ 'Which vitamin D dosage works best for my genetics?'
Get answers with links to research, explained in plain English you can actually understand and use.

Stay current with genomic science

New research comes out daily. Check relevance to YOUR genome instantly — no PhD required.

→ Study published today? Know in 60 seconds if it applies to you
→ Get notifications when new findings relate to variants you carry
→ Export citations and summaries to share with family or discuss on health forums
Stop wondering 'does this apply to me?' — get definitive answers based on your actual genetic data.

Simple interface, expert-level insights

Start with basic questions, go deeper when you want. You control the complexity level.

→ Beginner: Ask simple health questions, get clear yes/no answers with explanations
→ Intermediate: Explore gene interactions and understand how often variants appear in populations
→ Advanced: Access technical details, database references, and research-grade information when needed
Interface adapts to you — simple for everyday questions, detailed when you need to go deep.

This is for you if...

See yourself in any of these situations?

📊 You have genetic data collecting dust — Your 23andMe/AncestryDNA results sit in downloads. You paid for them — now put them to work daily.
🧬 You see health studies and wonder 'does this apply to me?' — Stop guessing. Get definitive answers in seconds based on YOUR genome, not population averages.
👨‍⚕️ You want to discuss genetics with your doctor but feel unprepared — Walk in with formatted data, citations, and confidence. Be an active participant in your health decisions.
⚡ You want answers now, not in months — 23andMe updates reports every 3-6 months. You can check new research the day it's published.
🔬 You're curious about your biology but not a scientist — Start with simple questions. Go deeper only if you want. No PhD required.

FAQs

My 23andMe data is from 2015. Is it too old?

Not at all! Your DNA doesn't change — whether your file is from 2010 or 2025, the variants are identical. Fun fact: Your genome has been the same since conception. We've analyzed files from as far back as 2010 and they work perfectly. We work with any year, any version (v3, v4, v5), and any provider: 23andMe, AncestryDNA, MyHeritage, or full genome sequences. What DOES change: research interpretation. That's why we update our knowledge base weekly with latest studies. We'll clearly explain which variants your specific file includes and any coverage limitations.

How do I know my genetic data is safe?

Your data is encrypted from the moment you upload it until you view results — no one in between, not even us, can read it. We use the same multi-layer encryption that banks use to protect financial transactions. Processed on secure servers without cloud upload unless you choose it. We never sell your genetic information to anyone — not advertisers, not insurance companies, not researchers. You can delete everything permanently with one click, anytime. We're GDPR compliant and follow strict privacy standards.

I'm not a scientist. Will this be too complicated?

Think of it like asking a friend who happens to know genetics. You type questions in normal language: 'Why does coffee make me jittery?' We give you clear answers based on YOUR genes, without technical jargon. If you want details, they're there. If you just want the practical takeaway, you get that. You control the depth.

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