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

"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
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