Find out your risk profile for over 50 complex multi-factorial diseases, which depend on the interaction of multiple genes and non genetic factors such as age, diet, lifestyle and exposure to environmental or risk agents.
Obtain personalized recommendation and with your doctor's help, act on modifiable factors in order to reduce and manage your overall risk.
go to healthgenome™
Find out your genetic risk to develop most of the more common cancer and, if necessary, perform specific follow-up tests with the aim of developing a preventive action plan.
If hereditary pathogenic variants are present, in fact, it increases the risk of developing cancer in your lifetime; knowing that is useful because it allows the implementation of screening strategies or risk reduction options through lifestyle modification or the use of therapies.
go to oncogenome™
Find out the presence, in your DNA, of mutations that while not causing illness for you, can be transmitted to your children, who may be sick instead, or that your children may in turn transmit: protect the health of your family.
carriergenome™ is a very useful report always, and in particular if you and your partner are planning to have children.
go to carriergenome™
Find out how your body metabolizes and answers to more than 150 drugs in common use; find out which effectiveness these drugs can have for you, whether a higher or lower dose than the standard dose is recommended for you, if you are particularly at risk to developing some side effects, or developing unfavorable interaction between a given drug and others, if it is favorite, for you , not to take a certain drug.
go to farmagenome™
Find out your genetic risk of developing breast and ovarian cancers, and if necessary, perform specific
follow-up tests in order to develop a preventive action plan.
If there are inherited pathogenic variants, in fact, the risk of developing breast and ovarian cancers during your life increases; being aware of it is useful as it allows the implementation of screening strategies or risk reduction options through targeted follow-ups, lifestyle changes or the use of therapies.
Furthermore, knowing the presence of one or more mutations also allows to establish the risk
of transmission to offspring.
go to oncogyngenome™
in addition to your report, you will receive the raw data of your DNA, the list of the 700,000 personal variants detected, in a standard format, which can be used to obtain further reports in the future, also from other personal genomics companies
keep them forever!
in addition to medigenome™ report, you receive your raw data, which you can use in this or future orders to purchase additional reports without paying genotyping costs!
you can also use the raw data with other personal genomics companies
if you have already purchased, in this order or in the past, other nowgenome™ tests with genotyping, or if you have your raw data provided by another personal genomics company such as 23andme, Ancestry.com, FTDNA, MyHeritage, 24Genetics and others, you do not need to repeat the lab test:
we can analyze your already available raw data to elaborate the medigenome ™ report,
and you can save money!
nutrigenome™ + sportgenome™ + allergenome™ + beautygenome™ + intelligenome™
+ healthgenome™+ oncogenome™+ carriergenome™+ farmagenome™
in order to obtain a complete package for your health
go to totalgenome™ package
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