In India, 1 in 9 people are likely to develop cancer in their lifetime.1 And no, it isn’t always bad luck, a poor choice, or an unhealthy lifestyle. Sometimes it's inherited, hidden in your DNA, while you have no idea about it.
What’s worse? By the time you’re diagnosed with cancer and find out that you’re carrying a high-risk gene mutation, it’s often too late. And the window for early, easier intervention closes.
But genetic testing can change that. A simple saliva or blood sample can tell you whether you carry inherited mutations that raise your cancer risk significantly. So that you can become aware of it before a diagnosis, and before it's too late to act.
This blog will guide you about genetic testing for cancer risk in detail: how it works, who needs it, and what to do with the results. So dive in!
About 10% of all cancer cases are caused by inherited mutations. Genetic testing checks the DNA found in every cell of your body to locate these mutations. These mutations can be either inherited from your family or occur spontaneously over time.2
If you inherit a mutation, it can significantly increase your personal risk of developing cancer.
Genetic testing currently covers risk detection for a range of cancers. Some common ones include:
You should consider genetic testing for cancer risk if:
A genetic test for cancer risk has the following benefits:
High-risk individuals can start screenings years earlier than standard guidelines recommend, giving an edge over those being diagnosed later.
Some people with high-risk mutations choose preventive surgeries or medications that significantly reduce their cancer risk. For example, preventive mastectomy reduces breast cancer risk by up to 90% in BRCA1/2 carriers. 10
If you test positive, your blood relatives can get tested too. It can also help you make better family planning choices. A result that helps one person can protect an entire family.
A negative result gives you clarity and can reduce anxiety around your family history.
Let’s take a look at the few simple steps involved in booking a genetic test for cancer risk:
1. Talk to your doctor first. Not everyone needs the same panel of tests. Your doctor or a genetic counselor can tell you which genes are relevant to your history.
2. Choose a certified laboratory. Tests should be done through accredited clinical labs. You can opt for LifeCell’s advanced genetic testing panels for cancer risk. These are highly accurate with expert-led panels and use state-of-the-art technology to detect genetic changes. To book your test, just visit our website, or you can even give us a call at 18002665533.
3. Once you have the test results, get them reviewed by your doctor or certified genetic counselors to understand them better and know your next steps.
Genetic testing for cancer risk won't tell you whether you'll definitely get cancer. But it does tell you whether your genetic makeup is quietly stacking the odds against you, before any symptoms show up.
The test itself is simple. But at the same time, the results can shape your health decisions for life. So if you have a family history worth paying attention to, don't wait for symptoms. Talk to your doctor and take the next step!
Yes. It's worth it if you have a strong family history of cancer or belong to a high-risk group. The results can directly change your screening schedule, treatment options, and preventive choices. For people with no family history and no known risk factors, routine testing is less necessary.
Genetic testing can show elevated risk for breast, ovarian, colorectal, prostate, pancreatic, stomach, thyroid, and skin (melanoma) cancers, among others. Each cancer type is linked to specific gene mutations.