KRAS-variant Registry

KRAS-variant Individual & Family Registry


MiraKind has opened a registry for KRAS-variant individuals and family members. The purpose of this registry is to collect information about changes in health over time for individuals with the KRAS-variant. Members of the registry will be asked to complete a detailed survey about his/her health every 4-6 months. In order to join the registry, an individual will need to have tested positive for the KRAS-variant or have a family member who has done so. Learn more.

If you are interested in participating in this research study, please complete our eligibility survey:
Apply to Participate!

Once you submit your survey, here is what you can expect:

  1. A MiraKind researcher will review your survey information, and you will then be sent the protocol and a consent to review.
  2. You will be given the contact information for a MiraKind researcher to ask any questions you may have about the study, before you consent.
  3. Once your questions have been answered you will be able to electronically sign the consent, and you will be enrolled in the study and sent your DNA collection kit.
  4. You will receive a follow up study specific questionnaire, as well as information on how to obtain individual results through a physician of your choice if you are interested in doing so.
  5. If you are not eligible for any MiraKind studies that are currently open but would like to stay updated on forthcoming studies, please join our e-newsletter.