A simple cheek swab reads the genes you were born with and shows how much of your health is already written
You carry 320000+ variants across clinically relevant genes. Our bioinformatics reports on the 368 genes that are clinically actionable and hands you the time to act. We inform. We never dictate.
368
Genes clinically reported
14
Pharmacogenomic genes
20k
Variants read per person
5
Areas from one sample
Typical DNA test
What it reads
Coding regions of known clinically relevant genes
A fixed list of common, pre-selected variants
Rare or unique variants
Read directly from your own sequence
Often missed only pre-chosen spots are checked
How many questions
All five areas from a single sample
Usually one area, per test
Dimension
Typical DNA test
Cent
What it reads
A fixed list of common, pre-selected variants
Coding regions of known clinically relevant genes
Rare or unique variants
Often missed only pre-chosen spots are checked
Read directly from your own sequence
How many questions
Usually one area, per test
All five areas from a single sample
A variant unique to you isn't skipped for not being on someone's pre-set list.
A single read covers all five areas of your report at once no separate test for each.
10–20% of some cancers are inherited. Reading those genes early means surveillance can start early and cancers found early have far better outcomes.
Cardiovascular disease is the single largest cause of death. Cardiomyopathies, arrhythmias and familial high cholesterol are often written in your genes.
Inborn errors of metabolism are individually rare but collectively common. Some surface only after years or under stress like pregnancy.
Same diagnosis, same prescription very different responses. Your genes shape how you process a drug, helping avoid toxicity.
You can carry a variant that never affects you but could affect your children. Knowing early gives couples real, unhurried choices.
One cheek swab, one report. Each area turns inherited risk into something earlier, and easier, to do something about.
Examples shown. All 368 genes are listed in the panel.
Some people process a drug so slowly that a standard dose becomes toxic. Reading those genes flags the risk before it's ever prescribed.
A few drugs only work once your body activates them. If yours can't, they do nothing — so you skip the wasted weeks, and the cost, and move to something that helps.
For medicines like the blood thinner warfarin, your genes shape the dose you need. Start where you should be, rather than adjusting after a reaction.
A few of the 14 markers, and what they help guide
Gene / Biomarker
Primary Drug Associations & Clinical Implications
Clopidogrel, a common blood thinner — and some antidepressants and acid-reflux drugs
Warfarin dosing the two genes that most shape how much you need
Codeine and other painkillers, tamoxifen, and many antidepressants
Fluoropyrimidine chemotherapy where a deficiency can cause severe toxicity
Thiopurines, used in leukaemia and autoimmune disease
Statins for cholesterol and the risk of muscle side effects
Clotting risk, relevant to oestrogen-based contraception and hormone therapy
Examples shown. All 368 genes are listed in the panel.
Some people process a drug so slowly that a standard dose becomes toxic. Reading those genes flags the risk before it's ever prescribed.
A few drugs only work once your body activates them. If yours can't, they do nothing — so you skip the wasted weeks, and the cost, and move to something that helps.
For medicines like the blood thinner warfarin, your genes shape the dose you need. Start where you should be, rather than adjusting after a reaction.
A few of the 14 markers, and what they help guide
Gene / Biomarker
Primary Drug Associations & Clinical Implications
Clopidogrel, a common blood thinner — and some antidepressants and acid-reflux drugs
Warfarin dosing the two genes that most shape how much you need
Codeine and other painkillers, tamoxifen, and many antidepressants
Fluoropyrimidine chemotherapy where a deficiency can cause severe toxicity
Thiopurines, used in leukaemia and autoimmune disease
Statins for cholesterol and the risk of muscle side effects
Clotting risk, relevant to oestrogen-based contraception and hormone therapy
Sign up for your genome through Cent. It takes a few minutes, and we take it from there.
A quick sample collected at our centre, no needle, no fasting, done in minutes.
Ready within 21 working days, all five areas in one place, written to be understood and acted on.
Genes reported
368
Variants analysed
20k
Areas covered
5
Sample type
Saliva
To your report
21 days
Genomics Profile
Sequencing Summary Overview
Genes reported
368
Variants analysed
20k
Sample type
Saliva
To your report
21 days
Areas covered
5
Your genome gives you information and time a head start, not a diagnosis. Your doctor decides, with you, using what your report reveals.
You leave with control, every time.
Your biology, made legible and useful.
Data you and your doctor can act on.
Sign up for your genome through Cent. It takes a few minutes, and we take it from there.
A quick sample collected at our centre, no needle, no fasting, done in minutes.
Ready within 21 working days, all five areas in one place, written to be understood and acted on.
Genes reported
368
Variants analysed
20k
Areas covered
5
Sample type
Saliva
To your report
21 days
Genomics Profile
Sequencing Summary Overview
Genes reported
368
Variants analysed
20k
Sample type
Saliva
To your report
21 days
Areas covered
5
Your genome gives you information and time a head start, not a diagnosis. Your doctor decides, with you, using what your report reveals.
You leave with control, every time.
Your biology, made legible and useful.
Data you and your doctor can act on.
The earliest decision is always the better one. Yours starts with a simple buccal swab.
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