MyGenome

Reads your whole genetic code once: inherited conditions, medicines, traits, and what you could pass to your children.
[ about MyGenome ]
Reads your whole genetic code once: inherited conditions, medicines, traits, and what you could pass to your children.
Providing:
  1. A full report, written in plain language
  2. Interpretation by geneticists, checked against international databases
  3. Findings you and your doctor can act on
  4. Updates over your lifetime, as scientific knowledge moves on
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[who is it for]
Right for you if
For adults, 18 and over
  • You would rather do one test now than add tests one at a time over the years
  • You are thinking about having children and want to know what you could pass on, even though you are perfectly healthy yourself
  • You want medication guidance included rather than bought separately
  • You want a result that can be read again in future as science advances, without giving another sample
[not this one]
This isn't the one you need if
  • You have one specific worry. If cancer or heart disease runs in your family, CancerRisk or CardioRisk answers that directly for EGP 60,000.
  • Your question is only about medicines. MyPharma is EGP 52,000. You don’t need the biggest test to get a good answer.
[About MyGenome]
What Does It Analyze?
We read your entire genetic code and look at thousands of gene changes. That covers:

Conditions passed down in families (650+)

Conditions you carry silently without being ill (225+)

Conditions caused by many things together (15)

How your genes affect your medicines (150+ markers)

Genetic traits (+50 traits related to diet, behavior, longevity, and more)

Ancestry insights

[test results]
What you'll get back
  • More than 650 inherited conditions checked
  • Whether you silently carry any of 225 conditions that could affect your children
  • Medication guidance based on 150 drug-response markers
  • 50 traits: how your body responds to different diets and exercise, sleep, and factors linked to longevity
  • Your ancestry
  • Your sequence is stored, so it can be read again as new discoveries are made
[carrier results]
What “carrier” actually means

Almost all of us silently carry a few conditions without being ill. On its own this changes nothing. It matters when both partners carry a fault in the same gene, and then there is a 1 in 4 chance in each pregnancy. That is why testing both partners is what makes the result meaningful.

[the limits]
What this test can't tell you
  • Your chances for common conditions like type 2 diabetes and high blood pressure. That is the scoring method MyHealthscore uses.
  • That you carry nothing. Reading the whole code is not the same as understanding all of it.
  • What will actually happen to your health. Genes are one input among many.
[Advantages]
Benefits of the test
For your doctor
The widest genetic picture from a single sample
Findings across conditions, medicines and what you carry silently
Data that can be read again as science advances
For you
You give a sample once
Know what you could pass to your children
A result that keeps its value over time
  • What you give Saliva No needles, no fasting, nothing to prepare
  • Doctor's referral Not needed Order it yourself, or start at a partner clinic
  • Genetic counselling Free before, extra after Our call centre helps you choose at no cost. A session with a clinical geneticist after your results is charged separately.
  • Collection Collected in 48–72 hours A nurse comes to you, or use a partner clinic. Results follow in 6 to 8 weeks.

Your health journey made simple

Five steps, from ordering to understanding your results.

01

Choose your test

Order online from anywhere in Egypt. No doctor’s referral needed. Not sure which one? Our call centre team will help you choose, free.

02

Book collection

A nurse comes to you at home, usually within 48 to 72 hours. Or give your sample at a partner clinic.

03

Give your sample

Saliva. A few minutes, no needles, and nothing to prepare beforehand.

04

The lab works

6 to 8 weeks. Every finding is reviewed by a geneticist against clinical databases before it reaches your report. That review is why it takes weeks, not days.

05

Results explained

A report in plain language, plus a version for your doctor. A session with a clinical geneticist is available separately.

[ common questions ]

Questions people ask before buying

You are never left alone with a result. A clinical geneticist can go through it with you and explain what it means in your situation, and for most findings there is something concrete to do next — earlier screening, closer monitoring, a change to a treatment plan, or knowing which relatives should be tested. Some results carry no action, and we will tell you that plainly rather than dress it up.

No. You can order any of our tests yourself, without a referral. If you would rather start with a clinic, we work with partner clinics in several locations and can point you to one.

Before you buy, yes — our call centre team has a medical background and will help you understand the tests and choose the right one, free of charge. After your results, a session with a clinical geneticist is available and is charged separately from the test.

Saliva. It takes a few minutes, there are no needles, and you do not need to fast or prepare in any way.

Collection is usually arranged within 48 to 72 hours, either at your home or at a partner clinic. Results take 6 to 8 weeks from the moment the laboratory receives your sample, because every finding is reviewed by a geneticist against clinical databases before it reaches your report.

For conditions that only appear in adulthood, the answer is usually no — and that is a deliberate choice, not an unhelpful one. A result a child cannot act on, and did not consent to, is theirs to decide about when they are old enough. Testing a child does make sense when a condition appears in childhood, or when acting early changes the outcome. If you are weighing this up, talk to us first and we will walk through it with you.

[our Professionals]
We offer you our team of professionals with whom you can arrange a genetic counselling consultation in person or online, to answer your questions and analyse your specific case.

Partner application

Become an iGenetx Partner