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Clinical Genomics Laboratory
About Clinical Genomics
The Mission of the Clinical Genomics Laboratory is to catalyze and drive genomic medicine implementation across Stanford and improve patient care.
The core purpose of the Laboratory is serving patients and providers from Stanford Health Care (SHC) and Stanford Children’s Hospital (SCH) by providing germline genomic testing for inherited disease diagnostics and innovative personalized medicine programs. The Laboratory includes three teams (wet laboratory, bioinformatics, interpretation) that are integrated with SHC operational management and ABMGG-certified faculty Laboratory Directors, which together develop and collaboratively implement ‘uniquely Stanford’ genomic tests with our clinical provider colleagues.
Pharmacogenomics Program
Please contact the Laboratory for more information on the Stanford Pharmacogenomics Program and the availability of PGx testing at StanfordCGP@stanfordhealthcare.org.
More information on the Stanford Pharmacogenomics Program will be updated soon.
Pharmacogenomics (PGx) Patient Frequently Asked Questions
Is this a research test?
No. This is a clinical test that is intended to help your providers tailor medication selection and dosing to you (precision medicine).
There are several people in my family with health conditions like cancer, neurological issues, diabetes, etc. Can genetic tests for these be added on?
No, if you have concerns about other genetic health conditions, referrals to other specialists are needed.
How much research is behind this test?
The genes included on this panel have lots of research supporting their effects on medications and strong evidence-based guidelines that we follow.
I have doctors outside of Stanford. How will they get the results?
You will need to give external doctors a copy of the results. If you have any questions in the future, you can reach back out to the PGx pharmacist.
Why should I get Stanford’s PGx panel compared to another lab’s PGx test?
The Stanford PGx panel was built by leading experts in the field of PGx, prioritizing the genes selected and medication recommendations with robust evidence and professional guidelines.
How does the test happen?
Step 1: Your provider will need to order the test for you in the Stanford system.
Step 2: The Stanford Clinical Genomics Lab will check your insurance coverage and report back to you what will be covered and if there is any financial responsibility for you to pay out of pocket
This step usually takes a few days and depends on the patient’s insurance. If an out-of-pocket cost is identified, testing will not proceed until approved by you.
Step 3: If you want to proceed with the test, the lab will mail a saliva kit to your home.If you have trouble with the saliva sample, you can request a blood draw instead.
Step 4: Follow the instructions in the saliva kit and mail the sample back to the lab.
Step 5: The lab will process the sample and release results within approximately 3 weeks.
Step 6: If your provider has requested it, you will receive a request from MyHealth to schedule a follow up visit to review your results with a PGx pharmacist. Please schedule this to take place 3-4 weeks after you have mailed back your sample.
Step 7: Your Stanford providers will use your results as part of the medication prescribing process to ensure you receive the best medications and doses for you based on your PGx test results.
What are the laws protecting me from discrimination based on my genetic information?
The Genetic Information Non-Discrimination Act (GINA) is a federal law that protects individuals from genetic discrimination in health insurance and employment. It does not apply to life insurance.
How will my genetic data be kept private?
Your PGx test data and results will be stored securely at the Stanford Clinical Genomics Lab, which is a requirement by CAP/CLIA and institutional policy. Please contact the Clinical Genomics Lab directly if you have any questions or concerns about DNA/data retention policies: stanfordcgp@stanfordhealthcare.org
Does my PGx genetic data get used for research?
Your de-identified PGx data and/or DNA sample may be used for internal Clinical Genomics quality improvement and/or test development projects. However, if any faculty member at Stanford wants to use your data for research it would need to be reviewed and approved by the Stanford Institutional Review Board (committee that oversees research to ensure ethical and safe practices).
Features
Stanford launches New Clinical Genomics Program
On March 21, the leaders of Stanford Medicine, Stanford Health Care, and Stanford Children’s Health came together for a ribbon-cutting ceremony to launch the new Stanford Clinical Genomics Program. The program brings the diagnostic power of whole-exome sequencing to children and adults with undiagnosed genetic conditions.
For Health Care Professionals
PHYSICIAN HELPLINE
Phone: 1-866-742-4811
Fax: 650-320-9443
Monday–Friday, 8 a.m.–5 p.m.
Fax: 650-320-9443
Monday–Friday, 8 a.m.–5 p.m.
Stanford Health Care provides comprehensive services to refer and track patients, as well as the latest information and news for physicians and office staff. For help with all referral needs and questions, visit Referral Information.
You may also submit a web referral or complete a referral form and fax it to 650-320-9443 or email the Referral Center at ReferralCenter@stanfordhealthcare.org.
HOW TO REFER
Fax a referral form with supporting documentation to 650-320-9443.
- Send referrals online
- Place radiology and lab orders
- View referral status
- Access medical records
Make An Appointment
You must be referred to the Clinical Genomics Program by a Stanford Medicine provider.
To make an appointment with a Stanford Medicine doctor, call 650-498-6000.
If you are a doctor and would like to make a patient referral, call 1-866-742-4811.