Establishing a sharing connection on 23andMe allows users to view one another's profile names, information from compatible reports, and the number and location of overlapping DNA segments. A sharing connection does not allow either person to search or download the other person's raw data, access their DNA Relatives list, or if applicable, view reports that require an additional consent, or view and download the other person’s Reports Archive.
When inviting someone to share, you can choose between two levels as described below:
Share Ancestry Only
- If you're related, see the location of matching DNA segments between yourself and the match, as well as any DNA relatives matches that you have in common. Furthermore, this shared segment information may be downloaded by your match through the DNA Relatives list download. Learn more.
- Compare your ancestries from the Ancestry Composition, Haplogroups, and Neanderthal Ancestry reports.
Share Ancestry + Health
- In addition to the capabilities above, you will be able to compare data from compatible health-related and traits topics.
- Reports that requires additional consent - such as Late-onset Alzheimer’s Disease*, Parkinson’s Disease*, and the BRCA1/BRCA2 (Selected Variants)* reports - cannot be shared between accounts.
- When you extend a sharing invitation, your profile name will be included in the sharing invitation. Once sharing has been established between two accounts, both full profile names will be visible in each other’s accounts. You can change your sharing level or stop sharing at anytime. Learn more.
- You would directly be sharing information about ancestral origins, family relationships (including a predicted relationship if applicable) and, if you've chosen that option, health-related information. Some people are comfortable sharing this kind of information, some are not — it's a personal choice.
- In the DNA Relatives feature, you can compare the shared DNA segments of two profiles you are sharing with even if those two are not sharing with each other. Similarly, the individuals with whom you share your profile may compare your DNA with that of other people they're sharing with. This aspect of sharing allows customers to compare people to each other and opens up new genealogical vistas by allowing customers to find evidence of family relationships.
- If you share with someone and you are related, your information will be included in their DNA Relatives data download. This information includes and is limited to: your profile name, your profile sex, the locations of the DNA segments you share, the results of your Maternal and Paternal haplogroups reports, and certain information that you choose to add to your DNA Relatives profile, if and only if you are participating in the feature.
- There is some chance that someone you are sharing with could learn something about you that you didn't directly share. For example, if you and someone you are sharing with have a matching segment of DNA that overlaps a health-associated gene, you might infer something about their genotype on the basis of your own, or vice versa. While it's important that we mention this possibility, in practice it is not easy to make inferences like this, and it doesn't happen very often.
Generally, we recommend sharing with people you are comfortable with. Sharing allows you to use more of the features on the website and adds a new dimension to what you can learn about yourself and your family. Many customers share openly with each other and have benefited from the experience. As you learn more about genetics and develop a finer sense of the issues involved, you might begin to share more openly yourself.
- You may not see data for an individual with whom you are sharing if that individual's data has not yet been loaded to his or her account. Even though you can't see his or her information, he or she will be able to see yours. Once his or her data becomes available you will be able to view it.
- Information for people already listed in your sharing list may disappear if they decide to discontinue the sharing connection or close their accounts.
*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. 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 other genetic health risk reports and carrier status reports, [visit https://www.23andme.com/test-info]