Between 10 and 18% of healthy people who undergo genetic screening get a clinically actionable result. Ordered through your physician and analyzed by Blueprint Genetics — part of Quest Diagnostics. Start with a free conversation.
Part of Quest Diagnostics
Some health risks don’t show up on blood tests, MRI, or echocardiography. They sit in your DNA — present from birth, invisible to all other diagnostics until the disease manifests.
Each panel is 11,900 SEK and included in Health Optimize membership. Your physician helps you choose the right one at the pre-test consultation.
The broadest preventive analysis. Cardiovascular disease, hereditary cancer, metabolism, and more — in a single analysis, for those who want the full picture.
Targeted analysis of inherited heart disease — cardiomyopathies, arrhythmias, aortopathies, and familial hypercholesterolemia.
BRCA1, BRCA2, Lynch syndrome, Li-Fraumeni and more — for those who want to understand their hereditary cancer risk.
More than 1 in 3 people are carriers of a recessively inherited disease without knowing it. For those planning a pregnancy.
Free 30-min consultation with your physician
Your physician orders the right panel — you can’t order it yourself
Saliva or blood sample taken at the clinic
Sample analyzed by Blueprint Genetics in Helsinki
Results review with your physician (45 min)
We think it’s more important that you make a well-informed decision than that you order a test.
Only medically actionable genes are analyzed — not all genes. You may carry variants in other genes that current science cannot yet interpret.
A risk variant means risk is elevated compared to the population — not that you will develop the disease. Penetrance varies dramatically between genes.
Genetic findings are never private the way other lab results are. We discuss implications, insurance, and consent at the pre-test consultation.
Our test sequences the full coding regions of thousands of clinically actionable genes. It’s processed in a CAP-accredited, CLIA-certified lab — the same standard used by Swedish hospitals for medical genetics. It reports only pathogenic findings, classified per international guidelines.
Consumer DNA kits sold online cost roughly 600–3,500 kr and are useful for ancestry or general curiosity — but in Sweden they can’t be used for medical decisions. Specialists and hospitals won’t accept consumer test results as the basis for diagnosis or treatment.
Here’s what you’re actually paying for:
| Online consumer DNA kits | Our clinical test | |
|---|---|---|
| Sample | Saliva | Blood (or saliva), drawn at a clinic |
| Technology | SNP microarray (~600,000 pre-defined positions) | Next-generation sequencing of full gene coding regions |
| Accreditation | Generally none for clinical use | CAP · CLIA · ISO 15189 — clinical-lab standard |
| Genes covered | Pre-selected SNPs across the genome | Thousands of clinically actionable genes, fully sequenced |
| Reporting | Raw variants, no medical interpretation | Only pathogenic / likely pathogenic variants, per international ACMG guidelines |
| Valid for medical decisions in Sweden | No | Yes |
| Includes physician time | No | Pre-test consultation + 45-min results review |
| Goes into your medical record | No | Yes — integrated at the clinic |
The 11,900 kr covers four things:
1. The clinical-grade test itself
2. A pre-test consultation with your physician — so you understand what you’re testing for before the result arrives
3. A 45-minute results review — findings explained, next steps mapped out
4. Integration into your medical record at the clinic, plus optional family counselling if pathogenic variants are found
If your goal is ancestry or curiosity, a consumer kit is the right choice — and cheaper. If your goal is actionable clinical information — hereditary cancer risk, cardiovascular risk, pharmacogenomics, family planning — consumer kits cannot deliver that. This test can.
