How it works
Three steps. One report your doctor can actually use.
No new kit. No saliva sample. No lab appointment. MarkerView starts from the file you already own — and the parts of your health that usually never get looked at in the same place.
From your file to your report
1
Upload the DNA file you already have
Your AncestryDNA or 23andMe account holds a raw data file you can download in about ten minutes. Upload it here. On Comprehensive you can upload both vendors' files, and we merge them into a single report for the highest marker coverage.
2
Add your medications, supplements & labs
Type in every prescription, every vitamin, every powder and capsule — the ordinary ones matter most. Attach your most recent Quest or Labcorp results if you have them. This step is part of MarkerView Comprehensive.
3
Get one plain-English report
A PDF arrives in your email, and it's waiting in your dashboard. Usually within a couple of hours. It's yours to keep, print, and hand to your physician.
What's actually in the report
Written to be read by you, and reviewed by your doctor.
Every section answers the same two questions: what does this mean, and what should I do about it? Nothing is left as a raw marker code you'd have to look up yourself.
Your genetic predisposition profile
The markers found in your file, grouped by what they affect, each written in plain English — with an honest note about how well your file actually covered that region.
Medication & supplement interactions
Every prescription and every supplement you entered, cross-referenced against curated drug monographs — including the combinations that only appear when the two lists are read side by side. Comprehensive.
Your lab work in context
Your most recent Quest or Labcorp results read alongside your genetics rather than in isolation, so a borderline number can be seen for what it is. Comprehensive, optional, no extra charge.
What's worth measuring next
The specific questions and tests worth raising at your next appointment — the part your physician can act on.
Sourced, not asserted
Marker mappings come from curated clinical databases and industry-standard open-source annotation tools. Drug–gene findings name the guideline behind them — CPIC or PharmGKB — with its PubMed ID, and a finding with no guideline behind it is labelled as such rather than dressed up.
Careful with the scary stuff
Consumer DNA arrays produce false alarms. Rare alarming calls are deliberately not headlined — they're framed for one action: a conversation with your doctor about confirmatory testing. Why →
Before you start
What you need, and what you don't.
You need: the raw data file from AncestryDNA or 23andMe (here's how to download it), an email address, and — for Comprehensive — your list of medications and supplements. A PDF of recent Quest or Labcorp results is optional.
You don't need: a new test kit, a saliva sample, a doctor's order, a subscription, or a phone call. MyHeritage support is coming; today it's AncestryDNA and 23andMe.
You're in control of the data the whole way: it's encrypted in transit and at rest, and you can delete your account and your data yourself at any time from Settings. The full trust answers →
Ready when your file is.
$10 for the DNA report. $20 for the full picture — DNA, medications, supplements and lab work reviewed together.