Likely lower blood serum level
Free while in early access
Already have a DNA file? See what else is in it.
You downloaded your raw data from 23andMe, AncestryDNA or another service and it has been sitting in a folder ever since. Upload it and we will read it properly — medication response, carrier status, nutrition, fitness, traits and ancestry — and send you our full analysis.
Free. No account. Delete it whenever you want.
Works with the file you already have
Upload the raw data file exactly as your service exported it. No need to unzip it first.
23andMeAncestryDNAMyHeritageFamilyTreeDNALivingDNAtellmeGen
Not sure which you have? Upload it anyway — we will tell you if we cannot read it.
- Encrypted with its own key, the moment it arrives
- Deleted permanently on request — key destroyed, not just hidden
- Never sold, never shared, never used for advertising
What we look at
Everything below comes from the file you already have, read against published, peer-reviewed research. These are example results, shown so you can see the shape of a report before you send us anything.
Some people break down common medicines faster or slower than most. Your file can show which group you fall into for several widely-used drugs — the kind of thing worth mentioning to a doctor before a new prescription. We read it against guidance written by the pharmacologists who set dosing standards, and it is free to read.
Example only — your report is built from your own file.
- Blood thinners, antidepressants and stomach-acid drugs CYP2C19 — clopidogrel, SSRIs, PPIsIntermediate
- Warfarin, a common blood thinner CYP2C9 + VKORC1 — affects the right doseTypical
- Statins, and muscle pain from them SLCO1B1Typical
- Medicines that damp down the immune system TPMT / NUDT15 — thiopurinesTypical
- Some chemotherapy medicines DPYD — fluoropyrimidinesTypical
- A chemotherapy medicine, and jaundice UGT1A1 — irinotecan, bilirubinTypical
- Some antibiotics and anti-malaria medicines G6PDTypical
- Anti-rejection medicines after a transplant CYP3A5 — tacrolimusIntermediate
- Codeine and many antidepressants CYP2D6 — your file cannot show this reliablyCannot be read
- Severe allergic reactions to certain medicines HLA-B — barely covered by consumer filesCannot be read
Two of these cannot be read reliably from a consumer file at all. We report them as unreadable rather than quietly calling them typical — an absent result is not a normal result.
Whether your file carries markers associated with recessive conditions. These matter most when two partners carry the same one, which is why people usually look at this before starting a family.
Example only — your report is built from your own file.
- Cystic fibrosis Affects the lungs and digestionNo variant found
- Sickle cell Affects red blood cellsNo variant found
- Tay-Sachs Affects the nervous systemNo variant found
- Haemochromatosis The body stores too much ironCarrier — one copy
- Alpha-1 antitrypsin deficiency Affects the lungs and liverNo variant found
- Factor V Leiden Affects how your blood clotsNo variant found
- Prothrombin G20210A Affects how your blood clotsNo variant found
Consumer files cover only a fraction of the known variants for these conditions. A clear result here is not an all-clear.
One thing we will not gloss over Consumer DNA files check only a few of the many known variants in genes like BRCA1 and BRCA2 — usually three founder variants, out of thousands. If you have a family history that worries you, nothing in a file like this, ours or anyone else’s, is reassurance. Please talk to a clinician about proper testing.
What you may absorb well and what you may not — the practical end of nutrigenomics, with the uncertainty stated rather than hidden.
Example only — your report is built from your own file.
Typical absorption
B12 absorption
Likely reduced conversion
Folate metabolism
Typical range
Iron handling
Likely efficient converter
Omega-3 conversion
Risk variants not found
Coeliac-associated markers
Around average
Sodium sensitivity
Power against endurance, how you respond to training, and how you recover. Useful for shaping how you train — not a ceiling on what you can achieve.
Example only — your report is built from your own file.
Leans towards power
Power vs endurance
Around average
Response to training
Lower predisposition
Soft-tissue injury
Around average
Recovery profile
The genuinely fun part. Small, specific and oddly satisfying to read about yourself — and the bit people screenshot and send to their family.
Example only — your report is built from your own file.
Likely tolerant
Lactose tolerance
Flush reaction unlikely
Alcohol flush
Likely a fast metaboliser
Caffeine metabolism
Moderate sensitivity
Bitter taste
Soapy taste unlikely
Cilantro aversion
Wet type likely
Earwax type
Around average
Photic sneeze
Slight morning preference
Body clock
Where your ancestors came from, computed against open reference panels rather than a proprietary black box.
Example only — your report is built from your own file.
- Northern & Western Europe 41%
- Southern Europe 24%
- Eastern Europe 18%
- Western Asia 11%
- Other regions 6%
Maternal line H1c
Paternal line R-M269
Neanderthal ancestry 2.1% of your genome — typical range is roughly 1–4%
Ancestry estimates are a comparison against reference populations, not a measurement. Different services use different panels, which is why their answers differ.
How it works
Upload your raw data file
The .txt or .zip your service gave you. It goes straight to encrypted storage — it never sits on our web server.
We check it and lock it down
Automated malware and format checks run within seconds. Your file is then encrypted with a key unique to it.
Your analysis arrives by email
Within one to two weeks, we email you a private link. The email itself never contains any of your genetic information.
What this is, and what it is not
What you get
- Our interpretation of your file against published research
- Plain statements of how confident we are, marker by marker
- A clear note when your file simply does not cover something
- Sources you can follow up yourself
What this is not
- Not a medical diagnosis and not a clinical test
- Not a substitute for advice from a doctor or genetic counsellor
- Not a basis for starting, stopping or changing any medication
- Not a complete picture — consumer files read a small slice of your genome
One thing we want to be blunt about: consumer DNA files check only a few of the many known variants in genes like BRCA1 and BRCA2. If you have a family history that worries you, a result from a file like this — ours or anyone else’s — is not reassurance. Please talk to a clinician about proper testing.
Upload your DNA file
Free while in early access. Your analysis arrives by email within one to two weeks.
Your file is with us
We will email your analysis within one to two weeks. Your reference is:
A confirmation is on its way to your inbox, with a link you can use to delete your data at any time.
Questions people actually ask
Is it really free?
Yes, while we are in early access. We are building this and want real files and real feedback more than we want your money right now. If we introduce paid tiers later, anything you have already received stays yours.
What do you do with my DNA?
We analyse it to produce your report, and nothing else. We do not sell it, share it with insurers or employers, hand it to advertisers, or add it to a research database. If you tick the optional updates box, we also re-analyse it when relevant new research appears — and you can switch that off at any time.
How do I delete it?
Every email we send you includes a deletion link that works for years. One click destroys the encryption key for your file, which makes it permanently unreadable — including in any backup copy of our file storage. We keep only a record that a deletion happened.
Why does it take one to two weeks?
Because a person checks the output before it reaches you. We would rather be slow and right than instant and wrong about something that matters this much.
Do I need an account?
No. You give us a file and an email address. Everything else happens through private links we email you.
Can I upload a file for someone else?
Only if it is your own data, or you have that person’s clear permission and the legal authority to act for them. Uploading another adult’s genetic data without their consent is unlawful in most places, and we take that seriously.