FAQs

How can this benefit my patient?

By comparing your patient’s sequence to the human genome reference sequence, IGS can detect DNA changes at almost every DNA base position. Further analysis of the individual genome sequence results can be used to identify:

  • Variants known, or highly suspected, to cause genetic disorders
  • Variants that appear to functionally alter genes that may play a role in genetic disorders or health concerns
  • Pharmacogenetic variants that have been correlated with differences in drug metabolism
  • Disease risk variants that have been correlated with increased risk of diseases, such as heart disease and diabetes

In some cases, individual genome sequencing may be able to provide information relevant to your patient’s current health status. In all cases, it will provide a library of your patient’s genetic information that can be leveraged for years to come.

Do you provide genetic counseling?

No. Illumina does not provide genetic counseling services. We recognize the tremendous value genetic counseling provides for patients both before and after any form of genetic testing and encourage doctors to use the additional expertise provided by these professionals.

To locate an experienced genetic counselor near you, visit www.nsgc.org.

Will health insurance cover the cost for an IGS service?

IGS may, or may not, be covered by your health insurance plans depending on the purpose of the test. Talk with your doctor and your health insurer for more information as each person’s case may be unique.

 
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