Ancestry $99 Health + Ancestry $199
no membership fees
no monthly subscription

Two easy ways to discover you.

Choose what's right for you.

Ancestry Features

Ancestry
Service

learn more

$99

Health + Ancestry
Service

learn more

$199

Ancestry reports 3 reports including: Ancestry Composition, Haplogroups, Neanderthal Ancestry
DNA Relatives (opt in) Find and connect with relatives in the 23andMe database who share DNA with you.
Health Features See full list of reports
Carrier Status reports* 35+ reports including: Cystic Fibrosis, Sickle Cell Anemia, Hereditary Hearing Loss  
Wellness reports 5+ reports including: Deep Sleep, Lactose Intolerance, Saturated Fat and Weight  
Traits reports 19+ 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. Ancestry
reports only
All
reports
Add Wellness, Traits and Carrier Status* reports Add later
for $125
Included!
You save $25.
Health + Ancestry discount: 10% off of each additional kit  
 

$99

add to cart

$199

add to cart
Ancestry Features

Health + Ancestry
Service

learn more

$199

Ancestry
Service

learn more

$99

Ancestry reports 3 reports including: Ancestry Composition, Haplogroups, Neanderthal Ancestry
DNA Relatives (opt in) Find and connect with relatives in the 23andMe database who share DNA with you.
Health Features See full list of reports
Carrier Status reports* 35+ reports including: Cystic Fibrosis, Sickle Cell Anemia, Hereditary Hearing Loss  
Wellness reports 5+ reports including: Deep Sleep, Lactose Intolerance, Saturated Fat and Weight  
Traits reports 19+ 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. All
reports
Ancestry
reports only
Add Wellness, Traits and Carrier Status* reports Included!
You save $25.
Add later
for $125
Health + Ancestry discount: 10% off of each additional kit  
 

$199

add to cart

$99

add to cart
 

Ancestry
Service

learn more

$99

Health + Ancestry
Service

learn more

$199

Ancestry reports 3 reports including: Ancestry Composition, Haplogroups, Neanderthal Ancestry
DNA Relatives (opt in) Find and connect with relatives in the 23andMe database who share DNA with you.
Carrier Status reports* Example reports include: Cystic Fibrosis, Sickle Cell Anemia, Hereditary Hearing Loss  
Wellness reports Example reports include: Deep Sleep, Lactose Intolerance, Saturated Fat and Weight  
Traits reports Example reports include: Male Bald Spot, Sweet vs. Salty, Unibrow  
See full list of reports
 

$99

add to cart

$199

add to cart

*Our tests can be used to determine carrier status in adults from saliva collected using an FDA-cleared collection device (Oragene·DX model OGD-500.001), but cannot determine if you have two copies of the genetic variant. Each test is most relevant for people of certain ethnicities. The tests are not intended to diagnose a disease, or tell you anything about your risk for developing a disease in the future. On their own, carrier status tests are not intended to tell you anything about the health of your fetus, or your newborn child's risk of developing a particular disease later in life.

The Cystic Fibrosis carrier status test is indicated for the detection of 28 variants in the CFTR gene and is most relevant for people of Ashkenazi Jewish, European, and Hispanic/Latino descent. The Sickle Cell Anemia carrier status test is indicated for the detection of the HbS variant in the HBB gene and is most relevant for people of African descent. The carrier status tests related to hereditary hearing loss consist of two tests – one indicated for the detection of two variants in the GJB2 gene which is most relevant for people of Ashkenazi Jewish and European descent, and one indicated for the detection of six variants in the SLC26A4 gene.

**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.

Choose your service

 

Ancestry

learn more

$99

Health + Ancestry

learn more

$199

Ancestry reports
DNA Relatives
Carrier Status reports*
Wellness reports
Traits reports
See full list of reports
 

$99

order

$199

order
 

Health + Ancestry

learn more

$199

Ancestry

learn more

$99

Ancestry reports
DNA Relatives
Carrier Status reports*  
Wellness reports  
Traits reports  
See full list of reports
 

$199

order

$99

order

Order Health + Ancestry today for $199 and save $25. Add Health reports later for $125 (total cost $224).

No membership fee
No monthly subscription

*Our tests can be used to determine carrier status in adults from saliva collected using an FDA-cleared collection device (Oragene·DX model OGD-500.001), but cannot determine if you have two copies of the genetic variant. Each test is most relevant for people of certain ethnicities. The tests are not intended to diagnose a disease, or tell you anything about your risk for developing a disease in the future. On their own, carrier status tests are not intended to tell you anything about the health of your fetus, or your newborn child's risk of developing a particular disease later in life.

The Cystic Fibrosis carrier status test is indicated for the detection of 28 variants in the CFTR gene and is most relevant for people of Ashkenazi Jewish, European, and Hispanic/Latino descent. The Sickle Cell Anemia carrier status test is indicated for the detection of the HbS variant in the HBB gene and is most relevant for people of African descent. The carrier status tests related to hereditary hearing loss consist of two tests – one indicated for the detection of two variants in the GJB2 gene which is most relevant for people of Ashkenazi Jewish and European descent, and one indicated for the detection of six variants in the SLC26A4 gene.