A new kind of knowledge.
A new kind of understanding.

The first and only genetic service available directly to you that includes reports that meet FDA standards for being clinically and scientifically valid.

The 23andMe Difference.

Receive an overview of your DNA – your 23 pairs of chromosomes – through detailed reports, tools and more.

Carrier Status reports*

If you are starting a family, find out if you are a carrier for an inherited condition.

Ancestry reports

Your DNA can tell you about your family history.

Wellness reports

Your genetics can help you make more informed choices about your diet and exercise.

Traits reports

Explore what makes you unique, from food preferences to physical features.

Tools

Use interactive tools to share, compare and discover more with friends and family.

Research

You can make a difference by participating in a new kind of research.

A new way to see yourself.

Genotyping is a great way to start understanding how your genetics can impact your life. It's a new filter. More knowledge to understand what makes you, you.

The world of genetics changes everyday – and we are committed to keeping you informed and knowledgeable so you can continue your genetic journey throughout your life.

Carrier Status reports*

35+ reports

Being a "carrier" means you "carry" one genetic variant for a condition. Carriers do not typically have the genetic condition, but they can pass a genetic variant down to their children. If both parents are carriers, there is a 25% chance their child will have the condition.

Understanding your carrier status helps you work with your doctor to prepare for the health of your future family. Important information about our Carrier Status Reports.

Reports include*
  • Cystic Fibrosis
  • Sickle Cell Anemia
  • Hereditary Hearing Loss
  • See all reports
See Sample Report
Ancestry Report

Ancestry reports

3 reports

Your DNA comes from all of your ancestors. In your DNA, we can find genetic traces of where your ancestors lived throughout history.

You also share DNA with people around the world today. You can choose to connect with them through our database. You will continue to find new relatives as our database of more than one million customers grows over time. Learn more.

Reports include
  • Ancestry Composition
  • Maternal & Paternal Lineage
  • Neanderthal
  • and DNA Relatives tool
See Sample Report

Wellness reports

5+ reports

When it comes to your wellbeing, your DNA is one part of the story that also includes your environment and lifestyle.

Find out how your DNA relates to your caffeine consumption, lactose digestion and your muscle type.

Reports include See Sample Report
Genetic Wellness Report
Genetic Trait Report

Trait reports

19+ traits

Find out your likelihood of having certain characteristics. See how your DNA affects your hair color, taste preferences and more. You can also compare your results to other 23andMe customers.

Reports include
  • Hair: Color, Loss, Curliness
  • Taste & Smell: Sweet vs. Salty, Bitter
  • Facial Features: Cheek Dimples, Unibrow, Freckles
  • See all traits
See Sample Report

Hi. Still have questions about our service?

Here are just a few of the things people frequently ask about 23andMe.
If you don't see your question here, get in touch with us.

How large is the 23andMe DNA database?

Will I be able to share information with my family?

Whom can I talk to about my carrier status* results?

*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.

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Carrier Status reports*

If you are starting a family, find out if you are a carrier for an inherited condition that could affect your children.

Ancestry

Your DNA can tell you about your family history. Learn where you came from, who you are related to and how you can find new genetic relatives.

Wellness reports

Your genetics can help you make more informed choices about your diet and exercise.

Trait reports

Explore what makes you unique, from food preferences to physical features.

What you can do

Use interactive tools to share, compare and discover more with friends and family.