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BE A PART OF THE GENOMICS SUPER STUDY 200


GAIN IMPORTANT INFORMATION ABOUT YOUR HEALTH
AND GET A FREE DNA TEST.

Enroll Now

Am I eligible? FAQ Education Portal


WHAT IS GENO4ME ALL ABOUT?


GENO4ME IS A PROVIDENCE RESEARCH PROGRAM THAT LOOKS AT HOW GENETICS CAN HELP
PERSONALIZE HEALTHCARE FOR YOU AND EVERYONE. YOUR PARTICIPATION IS KEY TO HELP
TREAT CANCER, HEART DISEASE, AND MUCH MORE.

ABOUT THE STUDY

Geno4ME is a study of how your genes can help personalize your healthcare. The
goal of Geno4ME is to increase the role of genetic information in improving
disease prevention and treatment for you. This information can benefit your
family members as well.

READ MORE →

WHAT YOU WILL LEARN

Discover what your genes can tell you about your risk for certain cancers,
cardiovascular diseases, and other inherited medical conditions. Find out if
there are certain medications that may not be as safe or effective for you
because of your genes.

READ MORE →


FINDING OUT YOUR GENETIC RISKS COULD HELP YOU AND YOUR PROVIDER MAKE A BETTER
PLAN FOR YOUR HEALTH.




FINDING OUT YOUR GENETIC RISKS COULD HELP YOU AND YOUR PROVIDER MAKE A BETTER
PLAN FOR YOUR HEALTH.


WHAT DO I HAVE TO DO TO TAKE PART IN THIS STUDY?

1. ENROLL ONLINE

First, you will be prompted to create a secure Providence Genomics account. Once
you verify your account, you will get access to the online consent portal. At
the end of the consent, you will be able to sign and complete your enrollment.

2. GIVE A DNA SAMPLE

After you submit your enrollment form, you will receive a saliva sample
collection kit in the mail. You can mail it back with your sample for free.

3. GET YOUR GENETIC RESULTS

You will be notified via email when your results are ready. You can view your
genetic results from your secure Geno4ME dashboard.

We're here to help
If your results show increased risk for inherited disease, a genetics
professional will help you understand your results and make a plan.


WHAT WILL YOU LEARN ABOUT YOUR GENES IN THIS STUDY?

1 in 50

people may have a genetic risk for inherited cancer or heart disease that
changes the way their doctor provides care.

~100%

of participants will discover if certain medications are safer or more effective
for them because of their genes.

3 in 4

people with genetic risk for hereditary colon or uterine cancer had no known
family history.


VISIT OUR EDUCATION PORTAL TO LEARN MORE ABOUT THE SCIENCE BEHIND YOUR HEALTH.


What is whole genome sequencing?
What are genetic variants and how can they affect you?
What are inherited diseases?
What is pharmacogenomics?
What are benefits of genomic screening?
See all of the education materials



This program is a collaboration with Genomic Data Network (GDN), a community
health ecosystem which facilitates clinical, research, and commercial
collaboration amongst its members and their patients.

CONTACT

Email: study.coordinator@health-system.xyz
Phone: (800) 333-3131

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