genome

AI-gestuurde genomische analyse — nu beschikbaar in de VS, VK en EU

Genomegenome
DNA Health Report

A DNA health report you'll actually understand — and want to act on.

Cancer risk, heart disease, drug response, nutrition, carrier status — all in one report. Cross-checked with 15 medical sources. Written so you can actually read it.

6 health categoriesCross-checked with 15 medical sourcesYour DNA is deleted after analysis
Trusted medical sources
ClinVarPharmGKBStanfordNIHGWAS Catalog
What You Get

Six categories. One complete picture.

Most DNA tests give you a sliver. We give you the full picture — from cancer risk to what supplements you actually need.

DNA health testing comprehensive visualization

Cancer Risk

BRCA1, BRCA2, TP53, CHEK2, PALB2, Lynch

Hereditary cancer screening across breast, ovarian, colorectal, and more. Confidence-rated findings with screening recommendations.

Heart Disease

LDLR, PCSK9, APOB, SCN5A, MYH7

Familial hypercholesterolemia, arrhythmia genes, and cardiomyopathy risk. Actionable steps you can discuss with your cardiologist.

Pharmacogenomics

CYP2D6, CYP2C19, CYP3A4, SLCO1B1

672+ medications mapped to your drug-response genes. Find out why a medication might not work for you before you take it.

Nutrition & Metabolism

MTHFR, CYP1A2, FTO, FADS1, MCM6

Caffeine metabolism, lactose intolerance, vitamin needs, and folate processing. A diet roadmap based on your DNA.

Carrier Status

CFTR, HBB, HEXA, SMN1, FMR1

Know what you could pass on. Cystic fibrosis, sickle cell, Tay-Sachs, and 50+ conditions checked before you plan a family.

Wellness & Traits

COMT, BDNF, CLOCK, ACTN3, ACE

Sleep quality, stress response, fitness type, caffeine sensitivity. The fun stuff that makes you, you.

Ready to see what your DNA says about your health?

Get Started
Why genome

Not another raw data dump

Most DNA tools give you data. We give you answers. Here's how genome compares to what's out there.

Health categories covered

genome: 6 (cancer, heart, pharma, nutrition, carrier, wellness)

23andMe: 2-3 (basic)

Promethease: Raw data dump

ChatGPT: Whatever it hallucinates

Medical sources

genome: 15 (ClinVar, PharmGKB, GWAS, gnomAD...)

23andMe: Proprietary only

Promethease: SNPedia (outdated since 2019)

ChatGPT: None (no database access)

Drug interactions

genome: 672+ medications, CPIC guidelines

23andMe: Not included

Promethease: Basic flags only

ChatGPT: Unreliable

Confidence ratings

genome: Yes (well-established / emerging / preliminary)

23andMe: No

Promethease: Magnitude score (confusing)

ChatGPT: No

Privacy

genome: DNA deleted after analysis

23andMe: Stored indefinitely (bankrupt)

Promethease: Owned by MyHeritage

ChatGPT: Sent to OpenAI servers

Report you can read

genome: Plain language + doctor-ready PDF

23andMe: Basic summaries

Promethease: "Gibberish" (Reddit)

ChatGPT: Conversational but unsourced

Sample Report

A report you'll actually want to read

Every finding comes with context: what it means, how reliable the evidence is, and what you can do about it.

Cancer Risk

BRCA2

rs80359550

Elevated Risk

One copy of this variant linked to increased breast cancer risk

Source: ClinVar

Heart Disease

LDLR

rs28942078

Elevated Risk

Familial hypercholesterolemia variant detected

Source: ClinVar

Pharmacogenomics

CYP2D6

rs3892097

Actionable

Poor metabolizer — codeine, tramadol, some antidepressants may not work as expected

Source: PharmGKB / CPIC

Nutrition

MTHFR

rs1801133

Actionable

Reduced folate processing — consider methylfolate supplementation

Source: GWAS Catalog

Carrier Status

CFTR

rs113993960

Carrier

Carrier of one cystic fibrosis variant

Source: ClinVar

Sample findings. Your report will be personalized to your genotype.

Health report dashboard showing genetic findings
Genomics data visualization with health insights

Your report includes findings across all 6 categories, confidence ratings, and a physician-ready PDF

Get your complete DNA health report in 2 minutes.

Same file you already have from 23andMe or AncestryDNA.

Get Started
How It Works

Three steps to your health report

1

Upload your DNA file

23andMe, AncestryDNA, Nebula, MyHeritage, or any VCF file. It takes 30 seconds.

2

We cross-reference everything

Your DNA is checked against ClinVar, PharmGKB, GWAS Catalog, gnomAD, and 11 more medical sources. Not a chatbot — a medical-grade pipeline.

3

Get your report

Cancer risk, heart disease, drug response, nutrition, carrier status, and wellness — all in plain language with a doctor-ready PDF.

Genome pipeline cross-referencing DNA with 15 medical sources

Our pipeline cross-references your DNA with 15 medical sources in real-time

Real Stories

What people discover in their DNA

Patient discussing DNA health report with doctor

Caught my cancer because of Promethease. Brought my report to push for a biopsy. Best money I've ever spent.

Reddit user, r/23andme

+156

After years of trying different medications, I finally did genetic testing and found out I have slow COMT and slow MAOA. Changed everything.

Reddit user, r/Nootropics

+20

I have no idea what I'm supposed to do with this gibberish that was sent to me. Speak to me like I'm 5.

Reddit user, r/promethease

+10

For the price of one month of random supplements, this tells you which ones you actually need.

Reddit user, r/biohackers

+26

6

health categories

672+

medications covered

15

medical sources

2–5 min

to get your report

FAQ

Common questions

Your DNA has answers.
We make them actionable.

Cancer risk, drug response, nutrition, carrier status — all in one report you can actually understand and share with your doctor.

2,400+ reports generated