codegen.eu · raw DNA analysis

Genetic research engine

A 25,000+ page deep-research report on your own DNA - your genome analyzed against 4,000+ topics (diseases and traits) and the scientific literature, using frontier models that processed over 1.5 trillion reasoning tokens across recent scientific papers. Search it like documentation. Summarized, ranked for relevance and grouped into reports with polygenic risk scores.

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Zero data retention

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

Your score vs population

lower riskhigher risk

rs10757278 W:2.40 49%

9p21 risk locus (G/G) - the most replicated common variant for coronary artery disease.

What you get

Raw DNA analysis you can actually use.

Upload the raw data file from your DNA test. 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 100k+ curated SNPs, variant groups and 4,000+ sub-reports, one per disease or measurement; every finding is scored against the general population, summarized in plain language and linked to the papers behind it.
Start FREE by reading all the short summaries. A single payment, with no subscription, unlocks the rest for good, with unlimited updates. Costs less than a month of a Premium streaming subscription.
Never stored. Your raw file is processed in memory and deleted within seconds; we keep no genetic data.

Reports

Almost every disease or measurement you can think of.

Inherited disease risk. Where your genetics sit for 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. A predisposition, never a diagnosis.
Metabolism and nutrition. Genetic tendencies behind your LDL cholesterol, vitamin D and B12 levels, how your body handles caffeine and lactose, body mass index, body fat, lean body mass and base metabolic rate.
Genes and medicines. Variants known to change how people respond to warfarin, statins and other drugs.
Psychological and everyday traits. 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. 4,000+ reports across 15 categories: inherited disease risk, metabolism and nutrition, genes and medicines, psychological and physical traits.

Polygenic risk scores

Scores computed by the book.

A polygenic risk score per established disease or measurement. GWAS associations are harmonized onto one effect allele, meta-analyzed across studies by inverse-variance weighting and reduced to a per-allele weight.
Your standing. Your allele dosages are summed, standardized against the population and ranked as an empirical percentile.
Honest about thin evidence. Reports resting on few variants are shrunk toward average and marked low confidence.
Published method. Grounded in science, with a peer-reviewed methodology. Follows Choi, Mak and O'Reilly, Nat Protoc 2020. A relative signal, not a diagnosis.

Search it like documentation.

Type a disease, drug, gene or rs-ID. Results come back ranked for relevance.
Narrow them down. By topic, by genotype frequency (common, infrequent, rare, very rare) and by risk band (good, info, warning, bad).
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.

Actionable insights. A plain-language summary for every genotype you carry, assembled from recent peer-reviewed papers plus dbSNP, the GWAS Catalog, ClinVar and OMIM.
With the numbers that matter. An impact score (0 to 4+), your genotype's frequency in the population, the gene and strand, and the references behind it.
Built from the original research papers, not second-hand summaries. Research current to 2026, from a deep-research pass over a vast corpus of papers exceeding 1.5 trillion tokens of reasoning and input.

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 impact score and references and shows up in search and report results next to ordinary genotypes.