BRCA1, BRCA2, and 12 additional breast cancer genes
Focused analysis of BRCA1 and BRCA2 — the most significant hereditary breast and ovarian cancer genes — plus PALB2, CHEK2, ATM and 9 additional variants.
Istanbul, Turkey
€380
Results in 10 days
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Postal saliva kit — no clinic visit required
Collect from home, post back in the pre-paid envelope. Results delivered digitally in 10 days.
BRCA1 & BRCA2 full sequencing
PALB2, CHEK2, ATM, RAD51C, RAD51D
BRIP1 & 6 additional variants
Lifetime risk estimate with benchmark
Mammography & surveillance recommendation
Best for: Women with a mother, sister, or daughter diagnosed with breast or ovarian cancer before 50
Browse every category covered in your Breast & Ovarian Cancer Panel — click a marker to see the action it unlocks.
Comprehensive sequencing of the most significant hereditary breast and ovarian cancer genes.
BRCA1
BRCA1 (chr17)
BRCA2
BRCA2 (chr13)
PALB2
PALB2 (chr16)
CHEK2
CHEK2 (chr22)
Every finding in your report comes with a concrete next step. Here's what your results can unlock.
Triggered by: Pathogenic or high-risk variant detected
15 yrs
earlier detection possible
Click to collapse
What this result reveals:
Which specific cancer types your variant predisposes you to, your lifetime risk percentage versus the general population, and the exact screening protocol recommended by international guidelines for your variant.
Begin enhanced surveillance: annual MRI, colonoscopy, or dermatology check based on your specific variant
Share your result with first-degree relatives — they carry a 50% chance of the same variant
Discuss with your GP which national screening programmes you may qualify for early entry
Stage 1 cancer has a 95%+ survival rate. Genetics can give you a 10–15 year head start on standard screening ages.
Triggered by: BRCA1/2, Lynch, or TP53 variant confirmed
−50%
risk reduction achievable
Click to see the full action protocol →
Triggered by: Any pathogenic variant identified
50%
relatives carry same variant
Click to see the full action protocol →
Every action protocol above is included in your digital report, reviewed by a specialist.
A parent, sibling, or grandparent was diagnosed. You want to know your hereditary risk before any symptoms appear — and get a screening head-start.
No alarming family history, but you understand that early detection changes outcomes. This test guides your screening decisions with data, not assumptions.
NHS or national programmes start at 50–60. Elevated genetic risk may qualify you for — and significantly benefit from — starting a decade earlier.
Not a raw data dump — a structured clinical report written in plain language, reviewed by your specialist before delivery, with every finding mapped to a concrete action.
Breast & Ovarian Cancer Panel — Genetic Report
Sample results · For illustrative purposes
35+
Genes sequenced
Hereditary variants
0
Pathogenic variants
Found
1
VUS found
Monitoring required
Low-Mod
Risk category
Population risk
BRCA1 status
Breast/Ovarian
BRCA2 status
Breast/Ovarian
PALB2 status
Breast/Ovarian
MLH1 status
Lynch Syndrome
+ 6 more markers in your full report
Report delivered digitally in 10 days from sample receipt. Reviewed by a specialist before release.
Inside your report
60-page clinical document
Executive summary — 1-page clinician overview
Full gene-by-gene findings with reference ranges
Your variant vs. 100,000-person population norms
Ranked intervention priority list by impact
Supplement & lifestyle protocol tailored to your results
GP & specialist summary letter (formatted for referrals)
Document library access via patient portal 24/7
Report formats included
Digital PDF
Download instantly from your portal
Patient portal
Interactive results, always accessible
GP referral letter
Formatted for your local doctor
Specialist letter
Category-specific clinical summary
Your patient portal is activated the moment your saliva kit is dispatched. Every result, action item, specialist message, and document — in one place, accessible 24/7 from any device.
Full report library
PDF + interactive results, always accessible
Secure specialist messaging
Direct line to your doctor, included free
Protocol reminders
Daily supplement and action item tracker
Access from any device
Web portal — no app download required
GDPR encrypted storage
Your data is private and deletable on request
Mobile-optimised
Full functionality on phone, tablet, desktop
Your action plan
2/5 done40% complete — tap any item to mark done
Share result with GP — screening letter generated
Send family summary letter to siblings
Annual clinical breast exam scheduled
PALB2 VUS — reclassification monitoring active
Book genetic counselling session (optional)
Portal activated instantly on kit dispatch. No app required — web-based access only.
Everything managed through your patient portal — no clinic visits, no waiting rooms.
Delivered to your door
ISO 15189 certified lab
Doctor reads your results
Manage everything online
Patient portal: Order your kit, track shipping, view results, message your specialist, and access your complete report — all from one secure dashboard, available on any device 24/7.
These are actual questions asked by patients about their Cancer Prevention results — answered in full by our specialists.
Dr. Aylin Kaya
MD PhDMolecular Genetics & Epigenetics Lead
Available for consultations Mon–Fri 9am–5pm (CET)
Dr. Mehmet Yilmaz
MDClinical Genetics & Pharmacogenomics Specialist
Available for consultations Tue–Sat 8am–4pm (CET)
Have a question about your specific situation? Our specialists reply within 2 hours.
Get in touch and your coordinator will send you the complete test guide, exact pricing, and your saliva kit within 2 hours. Free, no obligation.
Complete test guide & sample report emailed immediately
Saliva kit dispatched the same working day
Secure patient portal access on day of kit dispatch
Free 15-min pre-test call to answer all your questions
Results in 10 days — reviewed by a specialist before delivery
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Breast & Ovarian Cancer Panel
€380 · 10 days · Cancer Prevention
Start your consultation and a coordinator will guide you through the process — pricing, timeline, and everything you need to know.
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