23andMe makes a great gift for family members or friends. Our saliva collection kits offer a convenient method for DNA collection; most people who are able to spit can provide a sufficient sample for our laboratory to analyse.
This article discusses some things to keep in mind when purchasing 23andMe as a gift:
- Service Options
- Where to Buy
- Gift Wrap and Packaging Information
- Additional Important Information
- Common Questions
|Health + Ancestry Service||Ancestry Service|
The 23andMe® Personal Genetic Service can be purchased at:
23andMe Online Store Considerations
Kits purchased through the online 23andMe store are connected to your order’s email address. You must register your collection kit prior to mailing your saliva sample, however, your kit barcode will be emailed to the order email address if your unregistered kit arrives at the laboratory.
When placing your gift order through the 23andMe online store, please remember:
Order email address and phone number
The order confirmation email is sent to the address you provide during the order process, and the phone number is used to contact you in case of shipping problems. Many gift givers choose to enter their own contact information rather than the recipient information if they want the arrival of the kit to be a surprise.
Billing and shipping addresses
The online store offers the ability to enter independent billing and shipping addresses (one of each), so you have the option to send the kit(s) directly to the gift recipient if you wish. However, we do not offer the option to enter multiple shipping addresses.
When purchasing through Amazon.com you purchase your saliva collection kit and service through the retailer. You must register your collection kit prior to mailing your saliva sample in order to receive the 23andMe service. Kits available for sale through one of these authorized retailers are only intended for use within the United Kingdom.
Free gift wrapping or privacy packaging is available. To see these options, just check the box next to “Add gift message, gift wrap or privacy packaging” in the cart.
- Each individual who wants to participate in 23andMe needs his or her own saliva collection kit.
- Instructions regarding the sample collection process and 23andMe account creation and registration will be included in the kit.
- Return shipping is prepaid, and shipping instructions and materials are also included with the kit.
- The recipient of each kit will need to submit his or her saliva sample by the “Collect by” date printed on the side of the collection tube.
- Kits available for sale through one of the authorized retailers are only intended for use within specific the United Kingdom. Individuals must provide a sample and return the collection kit from the same country to which the kit was shipped by 23andMe.
- Saliva collection kits may not be sold or resold, but a kit can be registered by an individual other than the person for whom it was purchased. If the gift recipient does not want to participate, you may request a refund per our refund policy, or you can have another individual use the kit.
How can I ship to multiple addresses?
Shipping to multiple addresses in one order is not currently supported by the 23andMe online store.
Can I purchase a kit using a gift card or pre-paid card?
Yes, a gift card or pre-paid card from Visa, MasterCard, or American Express, can be used in the 23andMe online store. Just make sure that the gift card has enough available to funds to cover the total amount of the order (including shipping). If you are using a Visa gift card, you may need to register the card first and set a billing address prior to ordering.
Why isn't my shipping address being accepted?
If our store is unable to recognize your address, but you are certain that your shipping address is correct, feel free to proceed with your order. Alternatively, you may purchase through one of our authorized resellers.
Can I transfer ownership of a kit?
Yes, you can give an unregistered collection kit to someone else. It is during the registration process that a collection tube is connected with a specific person. If the collection tube has been registered, please contact us from the registered email address and we will outline the available options.
What is 23andMe’s refund policy?
23andMe has a 30 day refund policy; the kit cannot already be analysed or in the process of being analysed by the lab. Be sure to read the full policy.
*The 23andMe PGS test uses qualitative genotyping to detect clinically relevant variants in the genomic DNA of adults from saliva collected using a 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 varies 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. The Late-onset Alzheimer’s Disease genetic health risk report is indicated for reporting of the ε4 variant in the APOE gene and describes if a person has a variant associated with an increased risk of developing late-onset Alzheimer’s disease. The ε4 variant included in this report is found and has been studied in many ethnicities. Detailed risk estimates have been studied the most in people of European descent. The Parkinson’s Disease genetic health risk report (i) is indicated for reporting of the G2019S variant in the LRRK2 gene, and the N370S variant in the GBA gene, (ii) describes if a person has variants associated with an increased risk of developing Parkinson’s disease, and (iii) is most relevant for people of European, Ashkenazi Jewish, and North African Berber descent.
**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.