Finding inherited cancer gene markers in at-risk families
Part of Cancer clinical trials.
This study looks at DNA (genetic information) from people and families who may have an inherited risk for cancer. It aims to find new genetic markers that can help explain cancer risk and guide future care.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You (or your family) already had genetic testing or a genetics evaluation before
- Your results may show a known variant, an uncertain variant, or no harmful variant
- You may qualify if you have signs of inherited cancer risk (such as very early cancer, multiple cancers, or a strong family history)
- Family members—including children with a parent’s permission—can join if they can participate
- If needed, you may be asked to join even if you are not currently an MSK patient
- You must be able to understand and consent to the study (physical, cognitive, or mental health limits may exclude you)
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
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