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Interested in joining a visionary research team seeking to advance the utility of clinical genetic testing?
The iGAP Registry is both a retrospective and prospective observational registry documenting utility, clinical impact and patient experience for patients with or at risk of developing cancer, who obtain genetic testing.
The goal is to provide a platform to encourage private practice and academic physicians to collaborate in research on use of genetic testing in clinical practice.
The iGAP Registry will be an ongoing effort. Patient enrollment and subsequent follow up will occur over a minimum of 5 years. It is estimated that data from over 10,000 patients will be in the Registry.
The structure of the study is as follows:
All interested clinical practices performing genetic testing and counseling will be invited and encouraged to participate in the Registry.