Two easy ways to discover you.
Choose what's right for you.
Features |
Ancestry
Service
£79
|
Recommended
Health + Ancestry
Service
£149
|
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Ancestry Features
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Now with 1000+ regions
Ancestry reports
35+ reports including:
Ancestry Composition
,
Ancestry Detail Reports,
Maternal & Paternal Haplogroups,
Neanderthal Ancestry,
Your DNA Family
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Feature included
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Feature included
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DNA Relative Finder (opt in)
Find and connect with relatives in the 23andMe database who share DNA with you.
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Feature included
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Feature included
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Health Features
See full list of reports
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Genetic Health Risk reports*
5+ reports including:
BRCA1/BRCA2 (Selected Variants),
Alpha-1 Antitrypsin Deficiency,
Late-Onset Alzheimer's Disease,
Parkinson's Disease
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Feature not included
|
Feature included
|
Carrier Status reports*
40+ reports including:
Cystic Fibrosis,
Sickle Cell Anemia,
Hereditary Hearing Loss
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Feature not included
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Feature included
|
Wellness reports
5+ reports including:
Deep Sleep,
Lactose Intolerance,
Genetic Weight
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Feature not included
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Feature included
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Traits reports
25+ traits including:
Male Bald Spot,
Sweet vs. Salty,
Unibrow
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Feature not included
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Feature included
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Other Features
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Raw Data
Access your raw, uninterpreted genetic data file.**
Must not be used for medical or diagnostic purposes.
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Feature included
|
Feature included
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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.
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Ancestry
Reports only |
All
Reports |
Add Genetic Health Risk*, Carrier Status*, Wellness and Traits reports
|
Add later
for £90*** |
Included!
You save £20 |
Health + Ancestry discount:
10% off of each additional kit
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Feature not included
|
Feature included
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£79
|
£149
|
*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 each genetic health risk and carrier status report, visit 23andme.com/test-info/
**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 informational use and not for medical, diagnostic or other use. Consult with a healthcare professional before making any major lifestyle changes.
***Savings based on regular upgrade price of £90. We may offer special discounted upgrades from time to time.
Choose your service

Features |
Ancestry
learn more
£79
order
|
Health + Ancestry
learn more
£149
order
|
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checked | checked | |
Your DNA can tell you about your family history.
Ancestry Composition,
Ancestry Detail Reports,
Maternal & Paternal Haplogroups,
Neanderthal Ancestry,
Your DNA Family
|
||
checked | checked | |
Find and connect with relatives in the 23andMe database who share DNA with you.
|
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checked | ||
Learn how your genetics can influence your risk for certain
diseases. Example reports include:
BRCA1/BRCA2 (Selected Variants),
Alpha-1 Antitrypsin Deficiency,
Late-Onset Alzheimer's Disease,
Parkinson's Disease
|
||
checked | ||
If you are starting a family, find out if you are a carrier
for an inherited condition. Example reports include: Cystic
Fibrosis, Sickle Cell Anemia, Hereditary Hearing Loss
|
||
checked | ||
Learn how your genes play a role in your well-being and lifestyle choices. Example reports include: Deep Sleep, Lactose Intolerance, Genetic Weight
|
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checked | ||
Explore what makes you unique, from food preferences to physical features. Example reports include: Male Bald Spot, Sweet vs. Salty, Unibrow
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||
See full list of reports | ||
£79 order | £149 order |
Features |
Health + Ancestry
learn more
£149
|
Ancestry
learn more
£79
|
---|---|---|
checked | checked | |
Your DNA can tell you about your family history.
Reports include: Ancestry Composition,
Ancestry Detail Reports,
Haplogroups, Neanderthal Ancestry, Your DNA Family
|
||
checked | checked | |
Find and connect with relatives in the 23andMe database who share DNA with you.
|
||
checked | ||
If you are starting a family, find out if you are a carrier for an inherited condition. Example reports include: Cystic Fibrosis, Sickle Cell Anemia, Hereditary Hearing Loss
|
||
checked | ||
Learn how your genes play a role in your well-being and lifestyle choices. Example reports include: Deep Sleep, Lactose Intolerance, Saturated Fat and Weight
|
||
checked | ||
Explore what makes you unique, from food preferences to physical features. Example reports include: Male Bald Spot, Sweet vs. Salty, Unibrow
|
||
See full list of reports | ||
£149order |
£79order |
No monthly subscription
*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 each genetic health risk and carrier status report, visit 23andme.com/test-info/
See where your DNA is from out of 135+ regions worldwide – and more.
See where your DNA is from out of 1000+ regions worldwide – and more.
Learn the origins of your maternal and paternal ancestors and where they lived thousands of years ago.
Women can only trace their paternal haplogroup by connecting to a male relative - such as a father, brother, or paternal male cousin. This is because the paternal haplogroup is traced through the Y chromosome, which women do not inherit.
See how many Neanderthal variants you have, how that compares to others and what it means for you.
Discount does not apply to Ancestry kits.
Discount only applies to Health + Ancestry kits purchased within the same order and shipped to a single address. At least one full-priced Health + Ancestry kit must be purchased in order for subsequent kits to receive the discount.
Discounts, promotions and special pricing cannot be combined or used in conjunction with any other discount, promotion or special pricing and are not valid on previous purchases.
Get an overview of the diverse group of people who share your DNA.
Hereditary ThrombophiliaHereditary thrombophilia is a predisposition to developing harmful blood clots. These harmful blood clots most commonly form in the legs and can travel to the lungs.
Alpha-1 Antitrypsin DeficiencyAlpha-1 antitrypsin deficiency is a genetic condition that can lead to lung and liver disease. It is caused by decreased levels of the alpha-1 antitrypsin enzyme.