At a glance
You want disease-focused polygenic risk scores — 71 of them, each backed by a published study — for a one-time $20–$29.99.
You mostly want a wide range of light, wellness-style traits with a free starting tier.
What trait reports actually measure
Most consumer trait reports, from any company, are built on a small number of variants that a published study linked to the trait. For traits driven mainly by one variant, such as lactose tolerance, eye color, or the alcohol flush reaction, that works well.
For behavior and personality, individual variants explain very little of the difference between people. Reports on these traits are closer to entertainment than prediction, which is fine as long as they are read that way.
Disease risk is a different problem
Risk for common conditions like heart disease or type 2 diabetes depends on thousands of variants. Estimating it well takes a validated polygenic score, a reference population to compare against, and honesty about ancestry, since most scores were developed in people of European ancestry and predict less well in other groups (Martin et al., Nature Genetics, 2019).
That is what Genomisaur's Health Report is built for: 71 scores from published studies, each with its source and accuracy metrics, computed after imputing your file to about 30 million variants.
Pricing
Public list prices. Genomisaur Health Reports are $20–$29.99 one-time.
| Option | Price | What it is |
|---|---|---|
| Genomisaur Health Report | $20–$29.99 one-time | Up to 71 polygenic risk scores plus trait predictions |
| Genomelink | Free basic traits; paid unlock | Wellness and personality-style trait reports |
Competitor prices are public list prices from each vendor's site as of 2026 and change often; confirm on the vendor's site before purchasing.
Feature comparison
Side-by-side on the things that actually change what the product does for you.
| Feature | Genomisaur | Genomelink | Edge |
|---|---|---|---|
| Focus | Disease risk and health traits | Wellness, personality, and novelty traits | |
| Polygenic risk for common diseases | 71 published scores across 14 categories | Limited | |
| Source study for each result | Yes | Varies | |
| Free tier | No | Yes | |
| Subscription | No — one-time | Optional subscription |
What each one does well
Genomisaur
- Disease-focused, research-grade polygenic risk scores
- One-time price, no subscription
- Two-parent preconception report available
Genomelink
- Free starting tier
- Large catalog of light, wellness-style traits
Frequently asked questions
Can I use the same file I uploaded to Genomelink?
Yes. 23andMe, AncestryDNA, MyHeritage, and tellmeGen raw data files all work, as do single-sample WGS VCFs.
What is a polygenic risk score, and why does it matter for raw data?
Most common conditions — heart disease, type 2 diabetes, many cancers — are influenced by thousands of variants that each have a tiny effect. A polygenic risk score adds those effects up into one number and ranks it against a reference population. Consumer arrays measure hundreds of thousands of variants, and imputation fills in millions more, which is enough to compute these scores well. Looking at single SNPs one at a time, the way most free raw-data tools do, usually misses the bigger picture.
Is this medical advice?
No. Polygenic risk scores describe genetic predisposition relative to other people; they are not a diagnosis, and lifestyle and family history matter as much or more. Discuss anything concerning with a doctor or genetic counselor. Consumer arrays also miss many rare, high-impact variants, so a normal result does not rule out a hereditary condition. Most published scores, including ours, were developed in European-ancestry data, so results are less precise for people of other ancestries.
Informational, not diagnostic
Consumer genetic reports — ours, Genomelink's, and others — are informational. Carrier and polygenic risk results should be discussed with a qualified healthcare provider or genetic counselor before making medical or reproductive decisions.