More than 80 genetic markers that can increase the risk of developing breast, prostate or ovarian cancer have been found in the largest study of its kind.

The DNA of 200,000 people – half of them with cancer and half without – was compared, revealing an individual’s inherited risk of the diseases.

British scientists, who led the research, believe it could lead to a DNA screening test within five years.

They also hope it will boost knowledge of how the cancers develop.

The research was led by scientists at the University of Cambridge and the Institute of Cancer Research (ICR) in London and funded by Cancer Research UK (CRUK) and the Welcome Trust.

Study author Prof Doug Easton said: “We’re on the verge of being able to use our knowledge of these genetic variations to develop test that could complement breast cancer screening and take us a step closer to having an effective prostate cancer screening programme.”

Each of us is born with a genetic hand of cards passed down from our parents. This is called our genome and is made of three billion pieces of code made of just chemical letters: A, C, T and G. A single nucleotide polymorphism is a single letter difference in DNA between individuals.

We each have millions of variations and most of these seem benign. This study looked at more than 100,000 common differences found in at least one in 10 people.

By comparing cancer patients with healthy controls the scientists could identify genetic spelling mistakes that occurred repeatedly in the cancer group.

Forty nine new single nucleotide polymorphisms (Snps) were found associated with breast cancer, bringing the total identified to 76.

For prostate cancer, 23 new markers were found, bringing the total to 78. And for ovarian cancer, eight new regions were found, bringing the total to 12.

The scientists looked for common genetic variations – known as single nucleotide polymorphisms (Snps) – linked to the three cancers.

Each alteration raised the risk of cancer by a small amount. However, a small minority of men with lots of the markers could see their risk of prostate cancer increase more than fourfold and for women the breast cancer risk increase threefold.

By contrast, the test can also identify those with a smaller than average risk of developing the cancers.

A woman’s lifetime risk of breast cancer is one in eight, but among the 1% with lots of these newly identified genetic variations the risk rises to one in two.

The test could also help the one in 300 woman who carry a faulty gene known as BRCA1 or BRCA2. Two-thirds of them will develop breast cancer before the age of 80 and 45% who carry BRCA1 will get ovarian cancer.

At present the options to reduce their risks are limited – a double mastectomy or having their ovaries removed.

By combining the gene test for BRCA1 and BRCA2 with this extra genetic information, women who have a high number of the newly identified markers could find they have a nearly 100% risk of getting breast cancer.

In contrast, those with the protective versions of the genetic changes could see their risk drop to as low as 20%.

Dr Antonis Antoniou, CRUK senior fellow at the University of Cambridge, said: “Our research puts us on the verge of being able to give women a much more accurate picture of how likely they are to develop breast or ovarian cancer and would help to guide them about the most appropriate type and time of prevention or monitoring options for them.”

Prof Ros Eeles, from the ICR, said: “These results are the single biggest leap forward in finding the genetic causes of prostate cancer.

An AlphaBiolabs spokesperson said “We would like to congratulate the scientists involved in this remarkable discovery which will help the majority of mankind”. “We welcome this kind of research and hope to be part of the process when the technology filters down to commercial companies which will allow this kind of DNA test to become affordable to everyone”.