Genetic Testing in Partnership with Colorectal Cancer Alliance

Understand your inherited risk for colon cancer and other hereditary cancers, with support from certified genetic counselors at every step.
Save $10 with code FIGHTLYNCH
MyRisk Hereditary Cancer Test box enabling you to do at home genetic testing for cancer risk.  Includes BRCA1 and BRCA2 Testing.

jscreen’s Partnership With Colorectal Cancer Alliance

The Colorectal Cancer Alliance is fiercely determined to end colon and rectal cancers within our lifetime.  jscreen® shares the belief that everyone deserves access to testing that can protect themselves and their families from devastating genetic diseases.

Hereditary risk for colon cancer can pass through a family for generations without an obvious pattern. Genetic testing can help give you clear, direct answers that you can act on.

Get started with hereditary cancer testing today. Use code FIGHTLYNCH to save $10.

The Two Main Hereditary Colon Cancer Syndromes

Most hereditary colon cancers fall into one of two well understood categories. Both are identifiable through genetic testing and have clear management options when caught early.

Lynch Syndrome

Lynch syndrome is caused by inherited changes in DNA mismatch repair genes (MLH1, MSH2, MSH6, PMS2, and EPCAM). It's the most common hereditary colorectal cancer syndrome and also raises the risk of uterine, ovarian, stomach, and several other cancers. Colon cancer linked to Lynch syndrome often develops before age 50. Earlier and more frequent screening can allow cancers to be caught earlier. An estimated 1 in 279 people carry a Lynch syndrome gene mutation, but most are never diagnosed, missing the chance for early action.²

Familial Adenomatous Polyposis (FAP)

FAP is caused by a change in the APC gene. People with FAP typically develop hundreds to thousands of colon polyps beginning in their teens or twenties. The good news: genetic testing and early intervention can dramatically change the outcome. If a person has FAP and does not receive medical treatment, they have an almost 100% lifetime risk of developing colorectal cancer; however, the disease is highly manageable if it is found early through screening.³

Who Should Consider Hereditary Colon Cancer Testing?

1.

Family History of Colon Cancer

If a parent, sibling, or child has had colon cancer, especially at a young age, an inherited gene change that increases cancer risk may be involved and hereditary cancer genetic testing is recommended.

2.

Early Age at Diagnosis in the Family

Colorectal cancer diagnosed before age 50, in you or a family member, is a strong sign of the possibility of a hereditary syndrome like Lynch syndrome that increases cancer risk. Genetic testing can identify your inherited risk.

3.

Multiple Family Members with Colon Cancer

Two or more close relatives with colorectal cancer, especially across more than one generation, suggests an inherited cause that a comprehensive hereditary test can help identify.

4.

Personal Colorectal Cancer Diagnosis

If you've been diagnosed with colon cancer, genetic testing can clarify whether an inherited syndrome is involved, which can affect your treatment and help protect your family members.

5.

History of Uterine or Ovarian Cancer in the Family

Lynch syndrome raises the risk of uterine,ovarian and stomach cancers alongside colorectal cancer. A family history of these cancers is a strong indicator that genetic testing could be valuable.

6.

Multiple Colon Polyps

Developing many colon polyps at a young age can be a sign of FAP or other hereditary polyposis syndromes, which may be detectable through genetic testing.

Genetic Testing That Fits Your Needs

The health of your family depends on it

jscreen is a national genetic screening and education program offering access to comprehensive, at-home testing and genetic counseling.

Learn about hereditary cancer testing and find out what is right for you.

Hereditary Cancer Testing

Learn your risk for hereditary cancer, in a single test.

Why

Results are actionable and can be used for cancer prevention, early detection, and treatment.

What

jscreen is a national non-profit that offers access to comprehensive hereditary cancer testing. This test includes genes associated with Lynch syndrome (MLH1, MSH2, MSH6, PMS2, and EPCAM), BRCA1/2 and more than 60 other cancer predisposition genes. A genetic counselor reviews every case at intake and helps patients understand their results and take actionable next steps.

Who

This cancer test is designed for anyone who wants to understand their inherited cancer risk, and it works for people of all ancestries. It is particularly valuable for people with a personal history of cancer; people with a family history of cancer, especially at a young age; people with multiple relatives affected by the same or related cancers; and people of Ashkenazi Jewish ancestry due to their higher rates of certain mutations. While the test is available starting at age 18, jscreen typically recommends waiting until around age 25, depending on family history and other risk factors.

Save $10 with code FIGHTLYNCH

Why Genetic Testing Matters

A hereditary cancer test looks for inherited variants that raise your risk of cancer, giving you and your doctor real information to act on together. A positive result opens up options like risk-reducing surgeries, targeted therapies, and family planning support. A negative result, which means no pathogenic variants were found in the genes tested, may mean risk is no higher than average population risk, which can bring peace of mind to many people.

Actionable results

Clear, laboratory-interpreted findings with guidance on next steps.

Family Impact

Understanding your genetics helps protect siblings, children, and other relatives who may share your risk.

Early Detection Advantage

Knowing your inherited cancer risks enables proactive screening strategies that can help save lives.

Genetic Counseling Included

Every jscreen result includes access to a board-certified genetic counselor who will walk you through your report, answer your questions, and coordinate care recommendations with your physician.

Four Easy Steps to Access Genetic Screening from Home

a mailing envelope being received with a genetic screening kit inside

Order Your Kit

Register online and receive a saliva collection kit shipped directly to your home within a few days.

a mailing envelope being received with a genetic screening kit inside

Collect Your Sample

Provide a simple saliva sample at home, following the easy step-by-step instructions included in your kit.

a mailing envelope being received with a genetic screening kit inside

Lab Analysis

Your sample is analyzed at a CLIA-accredited laboratory using advanced sequencing technology across the full gene panel.

a mailing envelope being received with a genetic screening kit inside

Receive Results

 Receive your results within 3 to 4 weeks. You can choose to schedule a complimentary consultation with a certified genetic counselor to review your findings.

Costs and Insurance Coverage

jscreen was established on a simple but deeply held belief: that everyone deserves access to testing that can protect themselves and their families from devastating genetic diseases. We’re committed to working with you to ensure cost is never a barrier. 

Insurance Billing

Most commercial insurance plans cover hereditary cancer testing for individuals who meet criteria based on their racial or ethnic background, personal history, or family history. You will receive a personalized cost estimate from our lab partner. Your final cost depends on your family history and specific insurance plan. Our care navigators are here to help you work through the process and connect you with our financial assistance programs when needed.

Self-Pay Option

Prefer not to use insurance? jscreen offers a straightforward, competitive self-pay rate of $249, plus the upfront fee of $49, for a total of $298. This covers lab testing fees, physician review and test ordering, and access to our genetic counselors and care navigators throughout the testing process.