Welcome to Eiira Genetics!
We are pleased to offer our genetic profiling service to customers referred by our partners. When checking out, you can get a special discount by entering the code received from our partner.
To find out more about genetic prevention and related services, see the following pages:
Welcome to Eiira Genetics!
We are pleased to offer our genetic profiling service to customers referred by our partners. When checking out, you can get a special discount by entering the code received from our partner.
If you wish to learn more about genetic prevention and the products, these pages are designed to help:
Eiira Classic
A genetic test for hereditary cancer prevention
- Simple genetic test done at home
- Discover hereditary risks for 10 most common cancers
- Take actions with preventive measures
4990 kr
This is for you if:
You are worried about cancer
You or your family members have been diagnosed with cancer.
You are worried that cancer in your family will affect your children.
Pay now
4990 kr
Best value
6 Payments
879 kr/month
5269 kr total
12 Payments
460 kr/month
5516 kr total
Set-up fee SEK 0, administrative fee SEK 0/month, fixed annual interest rate 18.9%. 1) Effective interest rate 20.6%. The total amount includes the calculated credit amount of SEK 526 for Eiira Classic. Applies to a 12-month installment with Klarna. 2) Effective interest rate 20.5%. The total amount includes the calculated credit amount of SEK 279 for Eiira Classic. Valid for 6 months installment with Klarna. Credit provider and payee: Klarna Bank AB (publ) Sveavägen 46, 111 34 Stockholm. Amounts stated are an indication. Exact cost varies depending on the day of the month the purchase is made. For full terms and conditions, read more at klarna.com/en/terms.
Yes, it is easy. We will post a saliva collection kit and a return envelope to your home via Postnord. You simply spit saliva into the collection tube. If you need help, instructions are enclosed in the kit. Once you have collected saliva, you place the kit in the return envelope, which has a paid return label. You can then drop off the envelope at any Postnord service point.
The only other thing you need to do is to provide your details and our family’s medical history. The tools on our website will help you easily input the information. It is okay if you don’t provide your family medical history because you don’t know or you prefer not to.
The risk for 10 cancer types is mapped out by using the proven risk models and reference risk estimation data that are recommended in Swedish national guidelines. The below information is used as input to the mapping:
- The results of your genetic tests. You can find more information in the section "What is the technology behind the genetic test?"
- Your family medical history. Given the limitation of the current genomic science, your genetic test data alone cannot predict all risks. The family’s medical history contains much hereditary information. In some cases, family history alone can predict hereditary cancer risk. Therefore family medical history is used as part of the input.
- Information on you and your medical history. Personal information such as ethnicity and ancestry roots have an impact on our hereditary risks. Your lifestyle and medical history affect the risk level.
Note that the risks we report are hereditary risks. That is the risk that you inherited from your biological parents.
Bakom testet ligger en av de mest avancerade teknikerna som kallas Whole Exome Sequence (WES). Först analyseras ditt salivprov och alla DNA från könscellerna som är ansvariga för att generera dina proteiner fångas upp. Med “germinal” menas endast det DNA som du ärvde från dina föräldrar vid befruktningen. Därefter söker analysen efter eventuella patogena genförändringar (så kallade varianter) i DNA-data (dvs. dina hela exomdata).
I vår rapport ingår 50 gener som är kända för att orsaka en kraftigt ökad risk för att utveckla cancer. Urvalet av dessa 50 gener baseras på svenska nationella riktlinjer.
Because germline DNA remains the same during a person’s lifetime, you do not need to take another genetic test for your whole exome data. As genomic science and cancer prevention measures are constantly being discovered, you can enjoy these new advancements without taking another test.
First of all, we need to understand that the risk is the likelihood of developing cancer:
- Risk is not a diagnosis.
- Some people with high risk never have cancer.
- Similarly, people with low risk can still develop cancer.
Second, there are preventive measures to empower you. The report will inform you of proactive options available in Sweden. For many cancers, over 90% (close to 100% for breast cancers) survive if discovered early. The healthcare system has a number of monitoring programs to discover cancers early. We’ll inform you how to enter the Swedish healthcare system. There are also preventive healthcare partners that we can recommend to you.