top of page
shutterstock_1438256546.jpg

Hereditary Cancer Panel comprehensive multi-cancer panel to targeted panels for breast, ovarian, colorectal, prostate, melanoma and pancreatic cancer.

COMPREHENSIVE MULTI-CANCER RISK

Also available at 

Hereditary Cancer Panel comprehensive multi-cancer panel to targeted panels for breast, ovarian, colorectal, prostate, melano
APC, ATM1, BAP1, BARD1, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CDK4, CDKN2A, CHEK22, EPCAM3, HOXB13, MLH1, MSH2, MSH6, MUTYH, NF1
images.jfif
ATM1, BARD1, BRCA1, BRCA2, CHEK22, PALB2, PTEN, RAD51C, RAD51D, STK11, TP53

AT HOME LAB TEST FOR EARLY CANCER DETECTION ,DELIVERED ON DEMAND

ATM1, BARD1, BRCA1, BRCA2, BRIP1, CHEK22, EPCAM3, MLH1, MSH2, MSH6, PALB2, PTEN, RAD51C, RAD51D, STK11, TP53

Hereditary Cancer 

1

Order

No need to see a doctor

Click and order

Hereditary Colorectal Cancer (including Lynch syndrome) Panel

2

Sample

Easy quick Saliva or Stool sample 

Prepaid sample return by DHL / Royal Mail

Hereditary Melanoma Cancer Panel

3

Lab

Results in 7 days*

Results consultation included**

Beautiful Asian woman holding smartphone mockup of blank screen and shows ok sign on grey

*Coloalert 7 lab days excludes 1-3days shipping

Hereditary screening 10-14days 

**ColoAlert GP consultation for abnormal results at partner GP clinic. Hereditary Screening includes genetic counselling for abnormal results

Subscribe to Site

Thanks for submitting!

"BEST FOR PEACE OF MIND"

The team of HCPC registered clinical scientists at Informed Genomics will interpret your test results in accordance to well r

"ColoAlert goes further than the free, at-home NHS kits"

How IGL we Interpret genetic variants? At Informed Genomics, genetic variants are interpreted using the following methods:

"Non-invasive bowel cancer test catches illness early"

What are variants of unknown significance (VUS)? Variants of unknown significance are variants where there is either insuffi

"Only one in Europe to combine FIT`s capabilities with DNA markers in stools"

A genetic cause is suspected when the clinical features or family history include the following, in which case a hereditary c

As seen in the media

ColoAlert® is an award-winning next-generation colorectal cancer home screening test "
 

Our hereditary cancer clinical service at Informed Genomics aims to identify individuals at a higher-than-population risk for
bottom of page