Personalised breast cancer prevention

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Produktinformation

Know your risk. Protect your health.

Breast cancer can affect anyone – even without a family history. The AnteBC test provides a scientifically validated analysis of your personal breast cancer risk based on your genetic profile. Take control of your health early – simply, safely, and from the comfort of your home.

Your benefits at a glance

Genetic risk test via cheek swab – done at home
Calculation of your personal polygenic breast cancer risk

Get personalised guidance on when to start screening and how often
Learn actionable steps to reduce your risk
CE-certified, GDPR-compliant, and clinically validated
Optional video consultation – for personal guidance or to discuss your results

Who is it for?

Recommended for all women from age 30.
It is especially beneficial for women under 50, to identify those at higher risk early.
Perfect for health-conscious women, with or without a family history of cancer.
Accessible to everyone, everywhere through at-home genetic testing and digital medical prevention recommendations.

What is being tested?

The test calculates your breast cancer risk using a polygenic risk score (PRS), which combines the effects of 2,803 common genetic variants.

Unlike rare single gene mutations like BRCA1/2, polygenic risk is based on the interaction of many genetic variants – meaning your risk can be elevated even without a family history.

Your risk assessment also takes into account your age, ancestry, and sex, helping to create a personalised prevention plan with clinical recommendations.

What does this mean for you?

Your personal risk score compared to the general female population
Estimated probability of developing breast cancer within the next 10 years
Specific medical recommendations for prevention and early detection
A medical report for you and your healthcare provider

Additional important notes:

The test is not a diagnostic tool
A high risk does not guarantee disease – a low risk does not exclude it
Rare high-risk mutations (e.g. BRCA1, BRCA2) are not included
Based on UK Biobank data and CE-marked as an IVD in the EU and UK
The scientific models may evolve as new research becomes available

How it works

Order your test kit - Delivered to your home
Collect your sample – With a simple cheek swab
Send it back – Prepaid return envelope included

Receive your results online - Within 6 weeks, including your personalised prevention plan
Next steps with your healthcare provider - Start a tailored prevention program based on your results
If desired: Book a video consultation for personal support or to discuss your results – available via DoctorBox

Legal and scientific notes

As required by the German Genetic Diagnostics Act (GenDG), you will receive all mandatory medical information in writing before and after the test.

Before the test: Written pre-test counselling explaining the test, its purpose, and possible results
After the test: A digital report and a personalised prevention plan
Optional: If you prefer verbal counselling, you can book it separately via DoctorBox

Symptome

Why early prevention matters

• 1 in 8 women will be diagnosed with breast cancer during their lifetime
• Routine screening starts at age 50 – but 1 in 6 cases affect younger women
• Only 40% of breast cancers are detected early, though early detection raises survival chances to 99%

That’s why knowing your personal risk early can make all the difference. With the AnteBC genetic test, you gain clarity about your individual breast cancer risk – before symptoms appear. It’s a simple step that puts you in control of your health.

Ergebnisbericht

What’s included in your results

• At-home cheek swab test
Analysis of 2,803 genetic variants
Personal polygenic risk score
Breast cancer risk level vs. population average
10-year risk projection
Personalised prevention plan with clinical recommendations tailored to your profile
Medical report for healthcare providers
Scientifically validated advice to help you take action within your local healthcare system

Find answers to key questions:

What is my genetic risk level of breast cancer?
When and how should I start breast cancer screening?
Should I take additional preventive steps?
What can I do to reduce my risk of breast cancer?
Which changes or and symptoms should I watch out for?
What should my doctor know to support me best?

Your results give you clarity and control — based on science, tailored to you.

Häufige Fragen

Why should I start?

Breast cancer and related deaths can often be prevented through timely measures, even before symptoms develop. Personalised breast cancer prevention with genetic risk assessment can give early warning to women at risk even if there is no cancer in the family. It guides you towards tailored screening and prevention based on your risk levels. Each woman’s risk of developing breast cancer is highly individual. For those at high genetic risk, the likelihood of developing breast cancer can already be significant in their 30s and 40s. This should be carefully considered when planning screenings. By taking into account your unique characteristics – genetic composition, sex, age and ethnicity – your prevention plan is completely personalised.

Is this regulatory compliant?

Personalised cancer prevention is based on genetic risk tests provided by Antegenes. These tests are fully compliant with all regulatory bodies and government approved. Antegenes tests are clinical tests registered as CE-marked medical devices (in vitro diagnostics, IVD) in the EUDAMED database and UK MHRA Registry. These genetic risk tests were developed and validated using anonymised data from the UK Biobank.

What are the limits of the AnteBC test for assessing my risk of breast cancer?

The AnteBC test is not used to diagnose breast cancer, but shows your individual genetic risk. An increased risk does not mean that you will necessarily develop the disease - just as a low risk does not rule out a disease. The test only records your personal risk; the polygenic risk is not directly inherited and does not automatically apply to relatives. Rare high-risk mutations such as BRCA1, BRCA2, CHEK2 or PALB2 are not analyzed. The risk assessment is based on the current state of scientific knowledge and may change as a result of new findings. Different genetic models can provide slightly different results, depending on the gene variants taken into account and their weighting. Important: The results should always be considered in the overall medical picture - environmental and lifestyle factors also have a significant influence on the actual risk of developing the disease.

So funktioniert’s

Testkit bestellen

bequem nach Hause geliefert

Probe entnehmen

mit einem einfachen Wangenabstrich

Zurücksenden

Rückumschlag mit Porto inklusive

Ergebnisse online erhalten

in ca. 6 Wochen inklusive individuellem Präventionsplan

Mit deinem Arzt oder deiner Ärztin besprechen

starte dein persönliches Präventionsprogramm

Optional: Videoberatung mit einem Arzt oder einer Ärtzin

Für persönliche Fragen oder zur Ergebnisbesprechung via DoctorBox. Hier Videosprechstunde buchen!

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Personalised breast cancer prevention