and benefit from the human genome. These carrier reports are not intended to tell you anything about your risk for developing a disease in the future, the health of your fetus, or your newborn child's risk of developing a particular disease later in life. For certain conditions, we provide a single report that includes information on both carrier status and genetic health risk.

It’s easy. You decide what you want to know and what you want to share.When you opt in to participate in our research, you join forces with millions of other people contributing to science.

Your data is encrypted, protected and under your control. Each genetic health risk report describes if a person has variants associated with a higher risk of developing a disease, but does not describe a person’s overall risk of developing the disease.

Your ethnicity may affect the relevance of each report and how your genetic health risk results are interpreted. With reports like hair photobleaching and freckles, learn how your DNA can influence your physical features.Cilantro (coriander): is it delicious, or soapy? 23andMe is a consumer genetics and research company.

The PGS test is not a substitute for visits to a healthcare professional for recommended screenings or appropriate follow-up. For important information and limitations regarding each genetic health risk and carrier status report, visit 23andMe was founded in 2006 to help people access, understand and benefit from the human genome.We have more than three million genotyped customers around the world.You can make a difference by participating in research — online, from anywhere.
*The 23andMe PGS test uses qualitative genotyping to detect select clinically relevant variants in the genomic DNA of adults from saliva for the purpose of reporting and interpreting genetic health risks and reporting carrier status.

The Company offers DNA testing for inherited traits, genealogy, and possible congenital risk factors.

Your participation could help lead to discoveries that may one day make an impact on your own health, the health of your family and ultimately, people around the world.

By continuing to browse the site you are agreeing to our use of cookies. online, from anywhere. The three variants included in this report are most common in people of Ashkenazi Jewish descent and do not represent the majority of BRCA1/BRCA2 variants in the general population. It’s just a click away.Connect with relatives, known and new, near and far, when you opt in to DNA Relatives. Sign in with Apple. You can make a difference by participating in research —

The сompany enables people to gain insights into their ancestry and genetic makeup.

See the list of important policies below.

23andMe was founded in 2006 to help people access, understand

It’s convenient. Find out more

This report does not include variants in other genes linked to hereditary cancers and the absence of variants included in this report does not rule out the presence of other genetic variants that may impact cancer risk. See what your DNA might have to say about your taste and smell preferences.Endlessly fascinating and occasionally weird.

We have more than three million genotyped customers around the world.
This site uses cookies. No question is too big or small.

23andMe is the first and only genetic service available directly to you that includes reports that meet FDA standards for clinical and scientific validity. We are here to help with your questions. We have more than three million genotyped customers around the world.

23andMe was founded in 2006 to help people access, understand and benefit from the human genome. Our carrier status reports can be used to determine carrier status, but cannot determine if you have two copies of any genetic variant. 23andMe was founded in 2006 to help people access, understand and benefit from the human genome.

Warnings & Limitations: The 23andMe PGS Genetic Health Risk Report for BRCA1/BRCA2 (Selected Variants) is indicated for reporting of the 185delAG and 5382insC variants in the BRCA1 gene and the 6174delT variant in the BRCA2 gene. With genetic testing, you can discover how DNA might affect your ability to match a musical pitch, or even whether you hate the sound of chewing.Discover what makes you unique. The report describes if a woman is at increased risk of developing breast and ovarian cancer, and if a man is at increased risk of developing breast cancer or may be at increased risk of developing prostate cancer. 23andMe was founded in 2006 to help people access, understand and benefit from the human genome. No question is too big It is not intended to diagnose any disease. Click to read more. 23andMe was founded in 2006 to help people access, understand and benefit from the human genome.

It helps individuals to understand their own genetic information through DNA analysis technologies and web-based interactive tools.

The test is not intended to tell you anything about your current state of health, or to be used to make medical decisions, including whether or not you should take a medication, how much of a medication you should take, or determine any treatment.

Stay in the know about all things 23andMe. 23andMe is the first and only genetic service available directly to you that includes reports that meet FDA standards for clinical and scientific validity. Adding family tree information to your 23andMe profile is a great way to help your DNA matches figure out how they are related to you, and you can learn about how to do this (it’s different than the feature that I describe in this post) in the following tutorial: 23andMe Tutorial for Beginners; Conclusion

23andMe does not share any of your personal information with Google or Apple, including your genetic results


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