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.
Choose YourProtection Plan
Select the cancer screening package that best fits your health goals and family needs
Essential
$125 one-time kit fee
- GeneCancer screening panel
- BRCA1/2 analysis
- Basic hereditary risk report
- Digital report access
- Email support
- Screening recommendations
Premium
$125 one-time kit fee
- Everything in Essential +
- 108+ cancer gene analysis
- Lynch Syndrome testing
- Detailed screening plan
- Family risk assessment
- Genetic counselor consultation
- Priority 48-hour processing
- Risk comparison report
Family
$125 one-time kit fee
- Everything in Premium +
- Coverage for up to 4 people
- Bi-annual screening for all
- Family genetic risk mapping
- Shared family dashboard
- Dedicated account manager
- Lifetime report updates
- Prevention plan monitoring
Sample Report
Explore a real GeneCancer report with comprehensive cancer risk analysis and personalized recommendations
Report ID: GC-2024-789456
Sample Report — For Demonstration Purposes
Breast & Ovarian
Screening Recommendations
Cancer Risk Comparison
Get the Complete Report
Download the full report with all findings, screening recommendations, risk comparisons, and prevention strategies
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 Illumina next-generation sequencing — the same technology used by major cancer centers. Board-certified geneticists review every finding before your report is released.
Your Personalized Report — Yours for Life
In 2-3 weeks, 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 2-3 Weeks
Information that protects you and your family for a lifetime.
Frequently Asked Questions
Everything you need to know about GeneCancer
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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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