GeneCancerHereditary Risk Analysis
Comprehensive genetic testing analyzing 108+ genes associated with hereditary cancer syndromes. Get personalized screening recommendations and evidence-based prevention strategies.
Every Major Hereditary
Cancer Risk, Covered
GeneCancer doesn't screen for one type — it analyzes 108+ genes across all major hereditary cancer syndromes so nothing is missed.
Breast & Ovarian Cancer
BRCA1, BRCA2, PALB2, ATM, CHEK2, RAD51C, RAD51D
Lynch Syndrome & Colorectal
MLH1, MSH2, MSH6, PMS2, EPCAM, APC, MUTYH
Prostate Cancer
HOXB13, BRCA2, ATM, CHEK2, BRCA1
Melanoma & Skin Cancer
CDKN2A, CDK4, BAP1, MC1R, MITF
Li-Fraumeni & Rare Syndromes
TP53, PTEN, CDH1, STK11, SMAD4
Pancreatic & Gastric Cancer
BRCA2, ATM, PALB2, CDKN2A, CDH1, STK11
Your Family History Has
Answers In Your Genes
If cancer has appeared in your family tree, you deserve to know whether you inherited that risk — and exactly what to do about it.
"My mother had breast cancer. Am I at risk?"
Family history is one of the strongest indicators of hereditary cancer risk — and genetics can tell you exactly how much.
What the Science Says
BRCA1 and BRCA2 mutations are inherited — if your mother had breast or ovarian cancer caused by a BRCA mutation, you have a 50% chance of carrying the same mutation. Women with BRCA1 mutations have up to a 72% lifetime breast cancer risk compared to 12% in the general population.
GeneCancer analyzes BRCA1, BRCA2, PALB2, ATM, CHEK2, and 9 more breast cancer genes — giving you and your doctor a complete hereditary risk picture to build a proactive surveillance plan.
"Multiple family members have had colon cancer. Should I be worried?"
When colon cancer runs through families, Lynch Syndrome is often behind it — and it's one of the most actionable genetic diagnoses you can have.
What the Science Says
Lynch Syndrome is the most common hereditary colorectal cancer syndrome, caused by mutations in DNA mismatch repair genes. People with Lynch Syndrome have up to an 80% lifetime colon cancer risk — but with proper surveillance (colonoscopy every 1-2 years starting at 20-25), most Lynch Syndrome-related cancers are found early and treated successfully.
GeneCancer tests all five Lynch Syndrome genes (MLH1, MSH2, MSH6, PMS2, EPCAM) and provides a personalized colonoscopy schedule if a mutation is found.
"I'm a man. Do I really need hereditary cancer testing?"
Absolutely. Men carry BRCA mutations and face elevated cancer risks from them — and several hereditary cancer genes affect men just as significantly.
What the Science Says
Men with BRCA2 mutations have a 7% lifetime risk of breast cancer (vs. 0.1% normally) and up to 27% risk of prostate cancer by age 80. The HOXB13 gene dramatically raises aggressive prostate cancer risk. Lynch Syndrome in men raises colorectal, stomach, and urothelial cancer risk. These aren't just women's issues.
GeneCancer's male-specific reporting highlights prostate cancer risk genes, Lynch Syndrome variants, and BRCA2 — with PSA screening recommendations tailored to your specific genetic profile.
Knowledge is not fear — it's your most powerful prevention tool.
Know Your Hereditary RiskThe Gene That Changed
Everything
These aren't just stories — they're proof that hereditary cancer testing saves lives. Not someday. Now.
"Both my grandmother and aunt had breast cancer, but everyone assumed it was my mother's side we had to worry about. GeneCancer revealed I carry a BRCA2 mutation — from my dad. My sister tested positive too. We both started annual MRI screening. Eight months later, my sister's MRI caught a Stage 1 tumor that was completely invisible on mammography."
Stage 1 tumor caught. Lumpectomy, no chemotherapy needed. My sister is healthy today — and credits the test with saving her life.
"My dad and his brother both died of colon cancer before age 55. I was 46 when I finally did the test. They found an MLH1 mutation — Lynch Syndrome. My gastroenterologist immediately scheduled a colonoscopy. They removed three pre-cancerous polyps that were already there. Without that test, I might have waited until symptoms showed up."
Three pre-cancerous polyps removed. Now on annual colonoscopy surveillance. No cancer — and I intend to keep it that way.
"No obvious cancer history in my family, but my OB/GYN suggested genetic testing because I'm of South Asian descent and there are some hereditary patterns worth screening for. GeneCancer found a PALB2 mutation — which I'd never even heard of. It gives me a 35-58% lifetime breast cancer risk. I was 35. No one would have screened me for another decade without this test."
Started MRI surveillance at 35 instead of 40+. My oncologist says catching this early gives me the best possible options throughout my life.
Get GeneCancer with Essential Plan
GeneCancer is included in your Essential Plan subscription — along with 10 other genetic tests. No per-test fees. No surprises.
The Cost Comparison
GeneCancer individually
One-time purchase
$499
Essential Plan — all 11 tests
Monthly subscription
$69/mo
This test individually: $499. With your subscription: included at $69/mo along with 10 other tests.
GeneCancer is just the beginning
Your subscription unlocks all 11 tests. Here are a few more you get at no extra cost:
“My mother had breast cancer at 42. I finally got tested and found out I carry a BRCA2 variant. My doctor immediately put me on an enhanced screening protocol. That test may have saved my life.”
Jennifer K.
Chicago, IL
BRCA2 pathogenic variant detected
Choose YourHealth Journey
Comprehensive genetic testing subscriptions with your GeneMatrix AI DNA Kit included
Essential
Perfect for getting started
or $55/mo billed annuallySave 20%
What's included
- 10 Genetic tests per year
- 1 Annual cancer screening (108 genes)
- 1 Annual PGx (pharmacogenomics) test
- 77+ cancer types covered
- Basic pharmacogenomics (50 drugs)
- AI-powered health reports
- Basic risk assessments
- Personalized recommendations
- GeneMatrix mobile app
- Secure health dashboard
- Email support
- Downloadable PDF reports
- Ancestry insights
- Advanced predictive analytics
- Genetic counselor session
- Family health sharing
- Physician portal access
Premium
Most comprehensive coverage
or $71/mo billed annuallySave 20%
What's included
- 10 Genetic tests per year
- 2 Cancer screenings annually (188 genes)
- 2 PGx (pharmacogenomics) tests annually
- 120+ cancer types covered
- Full pharmacogenomics (350+ drugs)
- GeneMind mental health panel
- GeneDiet nutrition analysis
- Advanced AI health reports
- Comprehensive risk assessments
- Predictive health analytics
- Drug interaction alerts
- Priority email & chat support
- 1 Genetic counselor session/year
- Priority 48-hour processing
- Comprehensive PDF reports
- Family health sharing (2 members)
- Physician portal access
Family
Complete family protection
or $111/mo billed annuallySave 20%
What's included
- Coverage for up to 4 family members
- 4 Tests per member per year
- Bi-annual 188-gene screening for all
- 120+ cancer types per member
- Full pharmacogenomics for all
- GeneBaby pediatric panels
- Carrier screening for parents
- Family genetic risk mapping
- Cross-generational insights
- Hereditary condition tracking
- Shared family dashboard
- Dedicated account manager
- 4 Genetic counselor sessions/year
- VIP 24-hour processing
- 24/7 priority support
- Unlimited family sharing
Enterprise Solutions
Custom genetic testing programs for healthcare organizations, employers, and research institutions.
See Exactly WhatYou're Getting
Every single feature, side by side — so there are no surprises when you subscribe.
vs. purchasing 10 individual tests separately at ~$2,750/yr
vs. purchasing every Premium feature individually at ~$6,100/yr
vs. full individual plans for 4 family members at ~$24,400/yr
Questions about which plan fits your health goals?
Talk to a Genetic Counselor — Free ConsultationAll plans include your GeneMatrix AI DNA Kit
This is what knowing looks like
A real GeneCancer report doesn't just hand you gene codes. It tells you exactly what your risks are, what they mean for your life, and — most importantly — what to do about them.
Breast & Ovarian
3 genes analyzed
Your genes carry a significant increase in breast and ovarian cancer risk
You inherited a change in your BRCA1 gene — the gene responsible for suppressing tumors. When it's not working properly, cells can grow unchecked. Your lifetime risk of breast cancer is up to 72% (vs. 12.5% for the average person), and ovarian cancer risk is up to 44%.
- Your body's "tumor off switch" is partially missing
- Cancer can develop at a much younger age than average
- Other family members likely carry this same change
- Early detection with enhanced screening is proven to save lives
- Maintain healthy body weight (BMI 18.5-24.9)
- Exercise regularly: 150+ minutes moderate activity weekly
- Avoid tobacco and limit alcohol consumption
- Discuss chemoprevention options: Tamoxifen/Raloxifene for breast, Aspirin for colorectal
- Consider risk-reducing surgeries after thorough discussion with specialists
- Ensure all vaccinations current (HPV vaccine if eligible)
- Adhere strictly to enhanced screening schedule outlined above
- Keep detailed personal health records and family history
- Report any new symptoms promptly to healthcare team
- Consider joining hereditary cancer support groups
- Mental health counseling if experiencing anxiety about cancer risk
- Discuss findings with family in supportive, informative manner
Get Your Own Personalized Report
This sample only shows one patient's results. Your report is built entirely around your DNA — with your specific risk levels, your screening schedule, and your action plan.
From Home to
Life-Saving Clarity
Getting your hereditary cancer risk profile is easier than scheduling a doctor's appointment — and far more powerful.
Your Kit Ships to Your Door
A lab-grade DNA collection kit arrives within 2-3 business days. Inside: a sterile saliva collection tube, clear instructions, and a prepaid return envelope. No lab visit. No needle. No hassle.
A 2-Minute Saliva Sample at Home
Just spit into the collection tube — that's it. No needles, no clinic visits, no appointments. Cap it, seal the prepaid envelope, and drop it in any mailbox. Your DNA travels safely to our lab.
Our Lab Analyzes 108+ Cancer Genes
Your sample is processed in our CLIA-certified, CAP-accredited laboratory using our proprietary MassArray Sequencing technology — delivering ultra-precise variant detection across all 108+ cancer-related genes. Board-certified geneticists review every finding before your report is released.
Your Personalized Report — Yours for Life
In 5–7 days, receive a comprehensive, easy-to-read cancer risk report covering all 15+ cancer types. Share it with any oncologist, gynecologist, or primary care physician. Your results never expire — your DNA doesn't change.
Results in 5–7 Days
Information that protects you and your family for a lifetime.
Frequently Asked Questions
Everything you need to know about GeneCancer
Related Genetic Tests
Expand your genetic health insights with these complementary screening tests
GeneCore
Complete preventive genomics screening analyzing 130+ genes for cardiovascular, metabolic, and overall health optimization
GenePGx
Pharmacogenomics testing — discover how your genes affect cancer drug response for chemotherapy and targeted therapy
GeneMind
Mental health genetic screening for cancer patients — understand genetic factors affecting anxiety, depression, and treatment-related stress
Stop Wondering.
Start Protecting.
You can't change your genes — but you can change what happens next. GeneCancer gives you the knowledge to protect yourself and the family you love.
Covered by many insurance plans. HSA/FSA eligible. Share with any doctor, forever.
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