Genetic testing results study for rare diseases
Part of Cancer, Genetic & congenital clinical trials.
This study looks at how well different genetic tests (whole exome/genome sequencing and standard genetic tests) work for diagnosing rare genetic diseases and inherited cancer conditions. It may help confirm which testing approach provides the clearest results for families.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You (or a family member) have a genetic disease or an inherited tumor/cancer syndrome
- Your genetic testing was done at University Hospital Tübingen’s Institute for Medical Genetics and Applied Genomics
- Your genetic test date was between October 2016 and December 2020
- There are no listed exclusion requirements for this study
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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