23andMe Let's Talk about Genetics
Welcome to the 23andMe Genetics Learning Hub. Discover how genetics - as well as environmental, lifestyle, and other factors - can impact your likelihood of developing certain health conditions or having certain traits.
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Alzheimer’s Disease & Genetics
If you have a family history of late-onset Alzheimer's disease, learn more about genetic testing...Read more - about Alzheimer’s Disease & Genetics
Type 2 Diabetes & Your DNA
Learn what type 2 diabetes is, the symptoms to look for, and how genetics can play a role in how...Read more - about Type 2 Diabetes & Your DNA
Nonsyndromic Hearing Loss and Deafness, DFNB1
Learn about a type of inherited hearing loss called DFNB1, the genetics behind this condition,...Read more - about Nonsyndromic Hearing Loss and Deafness, DFNB1
Genetics and Weight
Learn more about how genetics and lifestyle impact your weight.Read more - about Genetics and Weight
Widow’s Peak Hairline & Genetics
The term "widow's peak" may sound grim, but a pointed hairline is just a genetic feature.Read more - about Widow’s Peak Hairline & Genetics
Unibrows & Genetics
Unibrows have graced the foreheads of some legendary faces. Whether you pluck your brows or let...Read more - about Unibrows & Genetics
Discover what you can learn from your DNA
Learn about topics like ancestry, wellness, traits, health predispositions (including genetic health risks), carrier status. You can discover how your DNA can provide insights into these topics as well.
23andMe’s reports provide genetic insights that can help you discover more about yourself and what makes you unique. With our Health Predisposition Reports*, find out how your genetics may influence the chances of developing certain health conditions. Our Wellness reports can help you understand how genetic factors may influence certain traits and conditions that can affect your quality of life. See how likely your unique appearance and senses are based on your DNA with our Traits Reports. Our Carrier Status Reports* can help you learn if you’re a carrier for certain inherited conditions, before you start a family.
23andMe ancestry reports and features give you the most comprehensive ancestry breakdown on the market, with up to 80+ personalized reports, coverage of more than 2000 geographic regions, and ancestry percentages to the 0.1%. We’ll also assemble a timeline of your genetic ancestry spanning over eight generations.
*23andMe health predisposition reports include both reports that meet FDA requirements for genetic health risks and reports which are based on 23andMe research and have not been reviewed by the FDA. The 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. It is not intended to diagnose any disease. Your ethnicity may affect the relevance of each report and how your genetic health risk results are interpreted. 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. 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. Our carrier status reports can be used to determine carrier status, but cannot determine if you have two copies of any genetic variant. 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. 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. 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. 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. 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. The PGS test is not a substitute for visits to a healthcare professional for recommended screenings or appropriate follow-up. Results should be confirmed in a clinical setting before taking any medical action. For important information and limitations regarding each genetic health risk and carrier status report, visit 23andme.com/test-info/