23andMe DNA Test Personal Genetic Service 90+Reports and atHome Saliva Kit

Sample Wellness Report: Genetic Weight
Find your genetic results and see how it might influence your wellbeing and lifestyle. Discover the habits that make the biggest weight difference in people with similar genetics.

ANCESTRY FEATURES: Ancestry reports

• 5 reports including: Ancestry Composition, Maternal & Paternal Haplogroups, Neanderthal Ancestry, Your DNA Family
• DNA Relative Finder: Find and connect with relatives in the 23andMe database who share DNA with you. (opt-in)

HEALTH FEATURES: Genetic Health Risk reports*

• 5+ reports including: Celiac Disease, Late-Onset Alzheimer's Disease, Parkinson's Disease Carrier Status reports*
• 40+ reports including: Cystic Fibrosis, Sickle Cell Anemia, Hereditary Hearing Loss Wellness reports
• 5+ reports including: Deep Sleep, Lactose Intolerance, Genetic Weight Traits reports
• 15+ traits including: Male Bald Spot, Sweet vs. Salty, Unibrow

OTHER FEATURES: Raw Data

• Access your raw, uninterpreted genetic data file.** Must not be used for medical or diagnostic purposes. Share, compare and discover more with friends and family
• Trace DNA through your close family and explore the genetic similarities and differences between you and family members.

*The 23andMe PGS test uses qualitative genotyping to detect clinically relevant variants in the genomic DNA of adults from saliva collected using an FDA-cleared collection device (Oragene-DX model OGD-500.001) for the purpose of reporting and interpreting genetic health risks and reporting carrier status. It is not intended to diagnose any disease. The relevance of each report may vary based on ethnicity. 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. These reports are 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 or how much of a medication you should take. 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 or anything about the health of your fetus, or your newborn child's risk of developing a particular disease later in life. For Gaucher Disease Type 1, we provide a single report that includes information on both carrier status and genetic health risk.

**This data has undergone a general quality review however only a subset of markers have been individually validated for accuracy. The data from 23andMe's Browse Raw Data feature is suitable only for research, educational, and informational use and not for medical, diagnostic or other use.

Before you can use 23andMe and see your reports, you must agree to 23andMe's Terms of Service (23andme.com/tos) at the time of registration of your 23andMe kit. Your use of 23andMe is further subject to 23andMe's Privacy Statement (23andme.com/privacy). For use in the USA only - kits shipped or used outside the US will be invalidated and no refund will be provided. Kits may not be redistributed or resold. Many conditions and traits are influenced by multiple factors. 23andMe reports are intended for informational purposes only and do not diagnose disease or illness.