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Genetic Disease Risk

Understand your inherited risk across 21 common conditions - common cancers, heart disease and stroke, raised cholesterol, type 2 diabetes, Alzheimer’s and more - from a single home saliva sample.

Genetic Disease Risk from £299

Conditions scored:

Heart disease
Type 2 diabetes
Breast cancer
Prostate cancer
Stroke
Alzheimer’s
Bowel cancer
Osteoporosis
+21 conditions scored
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Trustpilot
PKD Genetic Panel from £930
Medically reviewed by Ailidh Watson, Lead Genetic Counsellor·Last reviewed January 2026
21

Conditions scored

Cancers, heart, metabolic, brain and more

1

Saliva sample

At-home kit - no blood, no clinic, no fasting

~4 wks

Typical turnaround

Counsellor-explained, plain-English report

£299

One-off test

Includes genetic counselling before and after

Table of contents

Jeen
Cancer
Breast Cancer
Book now £930

What is a polygenic risk score?

Most common diseases aren’t caused by a single faulty gene - they’re shaped by thousands of tiny genetic differences, each nudging your risk up or down. A polygenic risk score adds all of those small effects together into one number: an estimate of how your inherited risk for a condition compares with the rest of the population.

Unlike carrier screening or hereditary-cancer panels that look for rare mutations, a PRS captures the common genetic background that everyone carries - the part conventional gene tests miss.

Important: a PRS estimates inherited risk only. It is not a diagnosis, not a prediction that you will or won’t develop a condition, and not a replacement for the NHS screening you’re entitled to.

For a step-by-step look at the science - from genome-wide studies to your personalised result - read our guide to how polygenic risk scores work.

21 conditions covered

Cancers: breast (women), ovarian (women), prostate (men), pancreatic, colorectal (bowel), melanoma.

Heart & circulation: coronary artery disease, stroke, atrial fibrillation, hypertension.

Cholesterol & lipids: polygenic high cholesterol, high triglycerides, low HDL, raised lipoprotein(a).

Metabolic: type 2 diabetes, body mass index (obesity risk).

Brain & nerves: Alzheimer’s disease (APOE-influenced).

Immune, digestive, bone & hormonal: inflammatory bowel disease, coeliac disease, osteoporosis, early menopause (women).

How it works

  1. Talk to a clinician - a free 30-minute consultation with a genetic counsellor confirms the test is right for you.
  2. Consent & collect - complete your online consent, receive your kit and give a simple saliva sample at home. No blood, no clinic, no fasting.
  3. Results & follow-up - your results are reviewed by a genetic counsellor and explained in plain English, with onward referrals if anything needs follow-up.

Why Jeen

  • Ancestry-specific scoring via Allelica - better calibrated across diverse backgrounds, not just European-ancestry data.
  • A genetic counselling consultation is included, before and after.
  • A simple at-home saliva kit - no blood, no clinic visit, no fasting.
  • A plain-English, personalised report, with a counsellor follow-up and onward referrals if needed.

Disclaimer! The information provided in this article is for educational purposes only. It is not a substitute for professional medical advice. Always consult your doctor or a qualified healthcare provider for advice on medical conditions or treatments. Sources used: NCBI, UK Kindney Association, NHS.

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What do we test for?

Know your genes, protect your future. Over 5,000 diseases are linked to genetic mutations. Early insights through genetic testing can help with prevention, early detection and personalised healthcare decisions.

Hereditary Cancer Risk

Testing 50 Genes Linked With Various Cancers

Hereditary Cancer Risk

Carrier Screening

Testing 1,008 Conditions That Could Affect Your Baby

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Other Genetic Conditions

Over 5,000 diseases are linked to genetic mutations

Other Genetic Conditions

Frequently Asked Questions

Are all the scores equally reliable?

No - and we’d rather be upfront about that. Polygenic scoring is more strongly validated for some conditions (coronary artery disease, breast cancer, type 2 diabetes, lipoprotein(a)) than others, and accuracy also varies with your genetic ancestry.

Why does ancestry matter for accuracy?

Most published polygenic scores were developed mainly from European-ancestry data and become less accurate for other backgrounds. Our models (via Allelica) are ancestry-specific, for a better-calibrated score across diverse heritages.

Do I need a GP referral?

No referral is needed - anyone aged 18+ can order directly. Polygenic risk scoring for these conditions isn’t routinely offered on the NHS, and this private test does not replace the NHS screening programmes you’re entitled to.

Is this a diagnosis?

No. A PRS estimates inherited risk only. It is not a diagnosis, not a prediction that you will or won’t develop a condition, and not a replacement for NHS screening - it’s a tool to help you and your doctor think about prevention earlier.

What conditions does the Genetic Disease Risk test cover?

It scores your inherited risk across 21 common conditions from a single saliva sample - including coronary artery disease, stroke, atrial fibrillation, type 2 diabetes, raised cholesterol, several common cancers (breast, prostate, bowel, ovarian, pancreatic and melanoma), Alzheimer’s disease and osteoporosis. Each is reported as your polygenic risk compared with the rest of the population.

How is a polygenic risk score different from BRCA or single-gene testing?

Single-gene tests such as BRCA or carrier screening look for rare, high-impact mutations in one gene. A polygenic risk score (PRS) instead adds up thousands of common genetic variants across your whole genome to estimate your risk of common, complex diseases. The two are complementary - a PRS measures the everyday genetic background that single-gene panels are not designed to capture.

How much does the Genetic Disease Risk test cost?

The test is £299, which includes your at-home saliva kit, laboratory analysis across all 21 conditions, a personalised report and a consultation with a genetic counsellor, included in the price. You can spread the cost with three interest-free Klarna payments of £99.67 at checkout.

How long do the results take?

Results are usually ready about four weeks after the laboratory receives your saliva sample. A genetic counsellor reviews every report and explains it in plain English, with onward referrals if anything needs follow-up.

What should I do if my risk for a condition is high?

A higher polygenic risk score is not a diagnosis - it means prevention may matter more for you. Your genetic counsellor will talk you through practical next steps, which might include lifestyle changes, earlier or more frequent screening, or a conversation with your GP. Knowing sooner gives you and your doctor more time to act.

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