Preemptive Genetic
Screening

每个人对药物的反应不同。有时这些差异是由基因引起的。先发制人的基因组筛查检查你的基因，以了解你的身体可能对某些药物的反应。

它可能预示着一种常见的处方药对你不起作用。这些信息，连同其他因素，可以帮助你的医生比简单的试错更快地为你匹配有效的药物。

All preemptive genomic screenings include pharmacogenomics.

View our PGx panel list of medications.

You can inherit an increased chance of developing a certain disease from your family. This is called a predisposition. Medically Actionable Predisposition (MAP) testing can tell you if you’re more at risk for certain health conditions than most people. It tests for genetic conditions such as cancer and heart disease.

This information empowers you and your doctor to take a proactive approach to your health. Knowing you’re genetically more likely to develop heart disease can get you started on a preventive plan now to keep your heart as healthy as possible.

Screening can also help your children and family members better understand their health risks through your results.

What to know
MAP检测是一项可选的基因检测。它会筛选与某些疾病相关的一组基因变异或变化。See the full list of conditions.

This test is not a replacement for diagnostic testing. It shows if you’re predisposed to a condition, not if you have it or are guaranteed to develop it. Predisposition means you’re more likely than most people to develop a condition.

Depending on your results, your screening may lead to additional testing, including diagnostic testing. Before signing up for MAP testing, talk about your concerns with your doctor. You can also speak to a genetic counselor to explore your options and get your questions answered.

To be eligible for genetic tests and screenings from Sanford Imagenetics, you must:

• Have an existing relationship with a Sanford Health primary care provider.
• Have an active卡塔尔世界杯预选赛比分account. You’ll need an account to receive your results.
• Be at least 18 years old

You’ll provide a blood sample
You’ll get a message through My Sanford Chart on where to go for collection.

You’ll receive your results
Our laboratory will test your sample and send your results to your provider. You’ll receive your results through My Sanford Chart. You can review your results any time by going to theMenuand selectingGenetic Profileat the bottom of theMy Recordsection.

A pharmacist will review your PGx results
We’ll reach out to your provider if there are any recommendations to adjust your medications.

You may receive a genetic referral
You’ll be referred for a genetic evaluation if you’re at a higher risk for a genetic condition.

Your health care team collaborates
If you consult with a genetic counselor or medical geneticist, your provider will receive information about your follow-up care and disease management plan.

We can coordinate family testing
如果你的家庭成员想要进行测试，你的基因咨询师可以帮助你。

Limitations:

• These screenings aren’t comprehensive and don’t identify all genetic variations or conditions.
• They should not be used as a replacement for genetic testing recommended by a health care provider.
• They may not find the cause of current health concerns or detect a variant that has been identified in your family.

Please tell your provider if you have any of the following:

• A current leukemia diagnosis
• Had a blood transfusion in the last 30 days
• Had a bone marrow transplant at any time in your life
• Had a liver transfer at any time in your life

If you’ve served, you may qualify for a discount. Contact us at (888) 424-2332 or (605) 312-GENE to learn more.

Our business hours are Monday through Friday from 8 a.m. to 4:30 p.m. CT.