Our products
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
12 installments for only 460 kr/month (5516 kr total)
Eiira Premium
A genetic test for hereditary cancer prevention
All benefits from Eiira Classic plus:
- Discovery of rare hereditary cancer risks
- Information covering 100% of your genome
- Enjoy lifetime updates of what future science can offer for preventive healthcare
9990 kr
12 installments for only 921 kr/month (11043 kr total)
Set-up fee 0 kr, administrative fee 0 kr/month, fixed annual interest 18.9%, effective interest 20.6%. Totals include estimated amount of credit of 526 kr for Eiira Classic and 1053 kr for Eiira Premium. Applies to 12 months of installments with Klarna. Creditor and payee: Klarna Bank AB (publ) Sveavägen 46, 111 34 Stockholm. The amounts shown are an indication. Exact cost varies depending on which day of the month the purchase is made. For complete terms and conditions, read more at klarna.com/se/villkor
What are the ten cancer?
Here is the list of the ten cancers:
Genes associated
To make this assessment, we have analyzed 50 genes in your DNA to identify the possible presence of disease-causing variants that are linked to an increased cancer risk. These genes have been selected based on their association with certain specific cancers or cancer syndromes. The table below shows the genes linked to the 10 different cancers covered by the analysis (i.e. the genes where we know that people carrying a disease-causing variant have an increased risk of cancer).
| Cancer type | Genes associated |
| Breast | BRCA1, BRCA2, PALB2, TP53, PTEN, CDH1, STK11, NF1, ATM, CHEK2, BARD1, RAD51C, RAD51D |
| Ovarian | BRCA1, BRCA2, PALB2, RAD51C, RAD51D, BRIP1, MLH1, MSH2, EPCAM, MSH6, PMS2 |
| Colon | MLH1, MSH2, MSH6, PMS2, EPCAM, APC, MUTYH, STK11, SMAD4, BMPR1A, PTCH, PTEN, NTHL1, POLD1, POLE, MSH3, TP53 |
| Prostate | BRCA2, HOXB13, BRCA1, MLH1, MSH2, MSH6, EPCAM, PMS2, ATM, CHEK2, PALB2, TP53 |
| Melanoma | CDKN2A, BAP1, CDK4, POT1, TERT, MITF1, MC1R, ASIP, TYR, TYRP1, TP53 |
| Kidney/Renal | VHL, FLCN, FH, MET, PTEN, SDHB, BAP1, SDHA, SDHC, SDHD |
| Thyroid | RET, APC, PTEN, DICER1, TP53 |
| Uterine | MLH1, MSH2, MSH6, PMS2, PTEN |
| Pancreatic Cancer | BRCA1, BRCA2, ATM, PALB2, MLH1 , MSH2, EPCAM, MSH6, PMS2, STK11, CDKN2A |
| Hereditary diffuse gastric cancer | CDH1, CTNNA1 |
How it works
1. Collect saliva at home
We’ll post you a saliva collection kit right to your doorstep. Simply collect the saliva and return it to us using the provided prepaid envelope.
2. Tell us about you
With our web tool, you can enter your information, including details about your family if desired. These inputs will be used to map out your genetic risks.
3. Get your profile
Download your profile report. In the case of a high risk, you have the option to consult with a genetic counsellor for further guidance
4. Stay updated
You can choose to stay updated on the latest risk mapping and preventive measures resulting from new discoveries in genetic science.
Compare Eiira Classic and Premium
| Features | Eiira Classic | Eiira Premium |
|---|---|---|
| Risk mapping for the ten most common cancers | ✅ | ✅ |
| Preventive measure for ten most common cancers | ✅ | ✅ |
| Updates for ten most common cancers | ✅ | ✅ |
| Future updates to cover other diseases | Limited | Unlimited |
| Lifetime updates of the latest discoveries in genetic science | Limited | Unlimited |
| Possibility to detect rare cancer variants | ⭐⭐⭐⭐ (medium) | ⭐⭐⭐⭐⭐ (most) |
| Genetic Sequencing Technology | Whole exome sequencing (WES) | Whole Genome Sequencing (WGS) | Choose your Eiira genetic test: | 4990 kr | 9990 kr |
Eiira customers
Check out what others have already done to prevent hereditary cancers with Eiira
Data privacy & security
Eiira takes your data privacy and security seriously
GDPR
Your data is securely housed in Sweden, adhering to the EU’s strict data privacy laws.
Exclusive use
Your data, exclusively used for your risk analysis, will never be shared with third parties without your permission.
Delete any time
You are the sole owner of your data and can request to delete your data at any time.
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