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Submit your story!

The HNRNP Family Foundation is made up of people impacted by variants in the HNRNP genes. We would love to highlight our community, so please share your story below and we will email you for a photo.

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Thanks for submitting!

Disclaimer: The information provided on this website is not intended to diagnose or treat a disease or disorder. Please direct any medical-related questions to your physician. The HNRNP Family Foundation is not responsible for any errors or omissions on this website.

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The HNRNP Family Foundation is a 501(c)(3) EIN 92-2394844

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