codegen.eu · raw DNA analysis (EST 2015)

Genetic research engine

A searchable report on your own DNA: your genome matched against 3,000+ reports (diseases and traits), each entry prepared from cited published studies and showing its sources. Search it like documentation. Summarized, ranked for relevance and grouped into reports, each with the variants and studies behind it.

Start FREE See a sample report

Free to start: search every variant and read the free reports. The full report is €24, one payment, no subscription; the total including VAT for your country is shown before you pay.

Zero genetic data retained

Coming back? There is no password. Upload the same raw data file again: your report is rebuilt, your favorites come back and anything you paid for stays unlocked. How logging in works

coronary artery disease

rs10757278 W:2.40 49%

9p21 risk locus (G/G). A common variant that many studies associate with coronary artery disease.

What you get

Raw DNA analysis you can actually use.

Upload the raw data file you already have. Files from 23andMe, AncestryDNA, MyHeritage, FamilyTreeDNA and others are supported; whole-genome sequencing files are not supported yet.
One searchable report. Your genotypes are matched against a catalog of 45,000+ SNPs, 130+ variant groups and 3,000+ reports, one per disease or measurement; every entry is summarized in plain language and linked to the papers behind it. Finding your way around codegen.eu
Start FREE with the nutrigenomics reports and search. A single payment of €24, with no subscription, unlocks the rest; the total including VAT for your country is shown before you pay. Your unlock does not expire while the service operates, and reports are updated over time at no extra cost.
We don't keep your file or your reports. The file is deleted as soon as your report is built; your report data is deleted when you log out or after 6 hours idle. What we keep

Reports

What studies report, from cancers to caffeine.

Common diseases. The variants in your genome that studies associate with type 2 diabetes, coronary artery disease, high blood pressure, atrial fibrillation and stroke; breast, prostate and colorectal cancer and melanoma; Alzheimer's and Parkinson's; celiac disease, rheumatoid arthritis, psoriasis, asthma and osteoporosis. Published research, not a diagnosis. Find out more: Modern diseases: cancers, heart disease and metabolic syndrome
Metabolism and nutrition. Variants that studies associate with LDL cholesterol, vitamin D and B12 levels, caffeine and lactose, body mass index, body fat, lean body mass and base metabolic rate. Only a lab test measures your actual level. Nutrigenomics: lactose, caffeine, vitamins and your genes
Psychological and everyday traits. Variants that studies associate with depression, anxiety, insomnia and sleep duration, migraine, resting heart rate, grip strength, physical activity and energy intake, male-pattern baldness.
Genes people ask about. APOE, MTHFR, HFE, Factor V Leiden (F5), LCT, CYP1A2, FTO, COMT and ACTN3, searchable by gene name or rs-ID.
Breadth. 3,000+ reports across 14 categories: common diseases, metabolism and nutrition, psychological and physical traits.

Search it like documentation.

Type a disease, gene or rs-ID. Results come back ranked for relevance.
Narrow them down. By category, by genotype frequency (common, infrequent, rare, very rare) and by relevance level (good, info, warning, bad). Searching the full report
Keep what matters. A rare-variants page collects your low-frequency genotypes; star anything to keep it in your favorites.

Summaries

Summaries from current research.

Practical takeaways. A plain-language summary for genotypes, assembled from recent peer-reviewed papers plus dbSNP, the GWAS Catalog, ClinVar and OMIM. Starts with simple explanations and expands in depth, facilitating research for curious users.
With the numbers that matter. A relevance score (0 to 4+), your genotype's frequency in the population, the gene and strand, and the references behind it. Variant geno card explained
Prepared from cited published studies. Every entry is prepared with AI assistance from the sources it cites, shows the studies behind it, and is updated when the catalog is refreshed. Research current to 2026. Limits of this report

Variant groups

Some variants only make sense together.

Capture complex interactions. A haplotype, or several variants in the same gene whose combined pattern is what matters.
Read like a single genotype. A variant group has its own relevance score and references and shows up in search and report results next to ordinary genotypes.