Skin Cancer Risk Test | Genetic Test
Ideal for health-conscious individuals—with or without a family history of cancer | Ages 18 and up
- AnteMEL
- Sample material
- cheek swab
- Analysed values
- 1 value
Colorectal cancer can affect anyone—even without a family history. With the AnteCRC Colorectal Cancer Risk Test, you’ll learn your personal genetic risk level. The scientifically validated test analyzes your genetic profile and helps you actively protect your health—easily, safely, and from the comfort of your home.

The test calculates your genetic risk for colorectal cancer using a polygenic risk score (PRS) that combines the effects of 91 common genetic variants. Unlike rare single-gene mutations, polygenic risk is based on the combination of many genetic factors—so your risk may be elevated even without a family history.
The analysis also takes age, ancestry, and gender into account to create a personalized prevention plan with clinical recommendations.
Result: Genetic counseling will be provided verbally. Alternatively, written counseling is possible if you give explicit consent. Your consent or refusal will be documented.
In accordance with the German Genetic Diagnostics Act (GenDG), you will receive all legally required information in writing before and after the test.
With the AnteCRC Colorectal Cancer Risk Test, you’ll identify your genetic risk early and can take proactive measures. The test gives you peace of mind, clarity, and a scientifically sound basis for your health decisions.
👉 Know your risk now – order the Colorectal Cancer Risk Test easily online.
Everything for sampling: collection material, instructions, a return envelope for the lab and your personal test ID for the DoctorBox app.
Home tests do not replace medical advice. If your values are abnormal or you have symptoms, please consult a doctor.
Genetics is one part of risk, lifestyle the other
The test calculates a polygenic risk score for bowel cancer from 91 common gene variants. Hereditary syndromes such as Lynch or FAP are not captured.
For people who want to decide when and how often to attend bowel cancer screening.
None. Blood in stool, changed bowel habits or weight loss need direct assessment, regardless of genetic risk.
The test calculates a polygenic risk score for bowel cancer from 91 common gene variants. Hereditary syndromes such as Lynch or FAP are not captured.
For people who want to decide when and how often to attend bowel cancer screening.
None. Blood in stool, changed bowel habits or weight loss need direct assessment, regardless of genetic risk.
The score compares personal risk with the population average. Lifestyle (smoking, alcohol, red meat, exercise) additionally influences risk and can be changed.
Plan screening with the result: stool test or colonoscopy, earlier and more often than from age 50 if risk is increased.
General orientation only. This does not replace medical advice or diagnosis.
Your kit arrives in neutral packaging, or you pick it up in Berlin.
Scan the test ID in the DoctorBox app so your report reaches you securely.
Capillary blood (virtually painless with Tasso+ on the upper arm if you like), swab, urine or saliva: the instructions guide you step by step.
The accredited lab analyses your sample and you receive the report with context, digitally.
Ideal for health-conscious individuals—with or without a family history of cancer | Ages 18 and up
Ideal for health-conscious women—with or without a family history of cancer | Ages 35 and up
For colon cancer screening
Ideal for health-conscious men—with or without a family history of cancer
After the sample arrives at the lab, analysis takes 2 to 10 days depending on the test. You are notified in the DoctorBox app as soon as the report is ready.
No. Every kit includes illustrated instructions. For capillary blood you use a lancet or, optionally, the Tasso+ device for nearly painless collection.
The parcel is neutral with no hint of its contents. Your invoice only shows DoctorBox.
Yes. Choose pickup at checkout. Your kit is usually ready within two hours.