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Colorectal Cancer (Powered by 23andMe Research) Reports and features that are “Powered by 23andMe Research” are developed by 23andMe scientists using data and insights gathered from thousands of customers who have consented to participate in our research. Genetic likelihood of developing cancer of the colon or rectum.
Your 23andMe reports will tell you about your genetic ancestry, and you may learn that you share recent ancestors with a group of people who identify as belonging to a particular ethnic group. However, DNA cannot estimate your “ethnicity” or your “race,” because understandings of these concepts are socially constructed and depend on context, place, and time.
23andMe offers three services: Ancestry Service, Health + plus Ancestry Service and 23andMe + plus Premium TM. All. services require submitting a saliva sample using our saliva collection kit that you send to the lab for analysis.Our . Ancestry Service helps you understand who you are, where your DNA comes from and your family story.
15 de mai. de 2024 · 23andMe's health reports included predispositions, carrier status, wellness, traits and a health action plan. Predispositions tested for Parkinson's disease, Type 2 diabetes, celiac disease and more.
Ancestry Service. £179 £129. Limit 3. Offer ends 16 June. Get genetic insights into your ancestry, traits and health that can help make it easier for you to take action on your health. 150+ personalised reports. Includes Ancestry Service. Add to cart. There is a lot to consider with genetic testing.
Accelerating research. Making an impact. On average, a customer who chooses to opt into research contributes to over 230 studies on topics that range from Parkinson's disease to lupus to asthma and more. With the help of our 23andMe community we believe we can accelerate research and make an impact with our genetic data.
Exome sequencing is an advanced genetic testing technique that focuses on decoding the exome of an individual's genome. The exome represents the protein-coding regions of genes, which make up only about 2% of the entire genome but contain the majority of genetic variants associated with disease risk. Exome Sequencing. Reports Δ.
