Patient-centered genomics-based care requires real genomics-based care coordination 
This 2-minute survey is NOT intended to be a deep academic analysis, but a initial guide to identifying the top industry issues for further discussion.
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Do you believe that your current healthcare system supports genetic-based care coordination effectively?

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Are you aware of any current initiatives or programs aimed at improving genetic-based care coordination in your healthcare system?

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If yes, could you briefly describe those efforts?
Check the box for each secondary provider you think should have full access to a patient's genomic information.

Does the EHR system your organization uses support easy genetic test result sharing?

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In the EHR, are genetic-based guidance and alerts (known as clinical decision support) that utilize genetic test results and other related clinical information available to all healthcare providers?

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Are family health history resources available for genetic-based care coordination in your healthcare system?

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What is the frequency, based on your knowledge (first or second hand), where collaboration exists among healthcare providers in coordinating care for patients with genetic conditions?

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In your opinion, what are the major barriers to achieving genetic-based care coordination in healthcare? Check all that apply.

If Other, could you briefly describe that major barrier?
End of survey
Survey results will be shared in a Moving Forward blog post when a significant number of responses are received.
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