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A genetic test for hereditary cancer prevention Simple genetic test done at home Detect hereditary risks for the 10 most common cancers Take preventive action Detect risks for rare hereditary cancers Information that covers 100% of your genome Lifetime updates on what future science can offer for health prevention. One year of free updates
This is for you if:
You are concerned about your cancer risks, including rare cancer risks
You want to benefit fully from current and future discoveries about your genes
You want to learn about your genetic predispositions
You wish to know your DNA to stay healthy
You wish to take full advantage of genome science discoveries to stay healthy
10548 kr total
11043 kr total
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.
For this purpose, we analyze 43 genes in your DNA for the absence or presence of pathogenic variants associated with an increased cancer risk. These genes are selected based on their known association with certain cancer types or cancer syndromes. The table below illustrates ten cancer types and their associated genes (i.e. genes where we know that individuals have an increased risk of cancer if they have a pathogenic variant).
|BRCA1, BRCA2, PALB2, TP53, PTEN, CDH1, STK11, NF1, ATM, CHEK2, BARD1, RAD51C, RAD51D
|BRCA1, BRCA2, PALB2, RAD51C, RAD51D, BRIP1, MLH1, MSH2, EPCAM, MSH6, PMS2
|MLH1, MSH2, MSH6, PMS2, EPCAM, APC, MUTYH, STK11, SMAD4, BMPR1A, PTCH, PTEN
|BRCA2, HOXB13, BRCA1, MLH1, MSH2, MSH6, EPCAM, PMS2, ATM, CHEK2, PALB2, TP53
|CDKN2A, BAP1, CDK4, POT1, TERT, MITF1, MC1R, ASIP, TYR, TYRP1, TP53
|VHL, FLCN, FH, MET, PTEN, SDHB, BAP1
|RET, APC, PTEN, DICER1, TP53
|MLH1, MSH2, MSH6, PMS2, PTEN
|BRCA2, ATM, PALB2, MLH1, MSH2, EPCAM, MSH6, PMS2
|Hereditary diffuse gastric cancer
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.
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.
Download your profile report. In the case of a high risk, you have the option to consult with a genetic counsellor for further guidance
You can choose to stay updated on the latest risk mapping and preventive measures resulting from new discoveries in genetic science.
|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
|Lifetime updates of the latest discoveries in genetic science
|Possibility to detect rare cancer variants
|Genetic Sequencing Technology
|Whole exome sequencing (WES)
|Whole Genome Sequencing (WGS)
|Choose your Eiira genetic test:
Your data is securely housed in Sweden, adhering to the EU’s strict data privacy laws.
Your data, exclusively used for your risk analysis, will never be shared with third parties without your permission.
You are the sole owner of your data and can request to delete your data at any time.