How do we get these numbers?

23andMe is a registered trademark of 23andMe, Inc. The use of the name and logo are for compatibility information only and does not imply approval or endorsement of Sequencing.com by 23andMe, Inc.

Compare the numbers

How do we get these numbers?

23andMe is a registered trademark of 23andMe, Inc. The use of the name and logo are for compatibility information only and does not imply approval or endorsement of Sequencing.com by 23andMe, Inc.

The world's only all-in-one genetic health screen

See what our customers are saying

See what our customers are saying

Featured In

Featured In

View All Included Conditions

World's most comprehensive rare disease screening

Rare Disease List
Buy Now
Buy Now

From our founder’s heart: Dr. Brandon Colby's story

Dr. Brandon Colby, founder of Sequencing.com, navigated through a challenging childhood plagued by a mysterious health condition—

Dr. Brandon Colby, founder of Sequencing.com, navigated through a challenging childhood plagued by a mysterious health condition—extensive blistering on his feet and hands, with no diagnosis in sight despite countless medical consultations and tests. His significant discovery was made possible by merging whole genome sequencing with the innovative Next-Gen Disease Screen (NGDS), a combination beyond the capability of any other existing test. This powerful approach finally uncovered the genetic culprit: a mutation in the KRT14 gene. 

This breakthrough not only provided Dr. Colby with much-needed clarity but also allowed him and his wife to make informed decisions about their family's future, understanding the implications of their genetic makeup. Dr. Colby's experience highlights the transformative impact of NGDS, showcasing its potential to replace fear and uncertainty with empowerment and precise genetic knowledge.

From our founder’s heart: Dr. Brandon Colby's story

extensive blistering on his feet and hands, with no diagnosis in sight despite countless medical consultations and tests. His significant discovery was made possible by merging whole genome sequencing with the innovative Next-Gen Disease Screen (NGDS), a combination beyond the capability of any other existing test. This powerful approach finally uncovered the genetic culprit: a mutation in the KRT14 gene. 

This breakthrough not only provided Dr. Colby with much-needed clarity but also allowed him and his wife to make informed decisions about their family's future, understanding the implications of their genetic makeup. Dr. Colby's experience highlights the transformative impact of NGDS, showcasing its potential to replace fear and uncertainty with empowerment and precise genetic knowledge.

Sequencing Includes

Whole Genome Sequencing

Carrier screening

Connective Tissue Disorders

Autoimmune Disorders

Sequencing

Cost on your own

$2,500

$350

$1,450

$1,450

$6,740

*

N/A

$990

$389

Screen For 15,000+ Conditions

Developmental Disorders

More insights. Lower cost. Total DNA clarity.

Get Whole Genome Sequencing with 15,000+ condition screening, health reports, and lifetime data storage—all for one price. No other company offers this much insight and lifelong access in one product.

* No other company on the market provides screening for 15k+ conditions in one product to consumers for any price.

More insights. Lower cost. Total DNA clarity.

Whole Genome Sequencing

Connective Tissue Disorders

Autoimmune Disorders

Carrier Screening

Sequencing Includes

Sequencing

Cost on your own

$350

$1,450

$1,450

$990

N/A

$2,500

$6,740

*

$389

Screen For 15,000+ Conditions

* No other company on the market provides screening for 15k+ conditions in one product to consumers for any price.

Based on Blueprint Genetics, Invitae, Natera, and Prevention Genetics as of July 2025.

Developmental Disorders

Based on Blueprint Genetics, Invitae, Natera, and Prevention Genetics as of July 2025.

Sequencing.com analyzes your entire genome to screen for 15,000+ diseases, conditions, traits, and medication reactions, covering almost every disease with a known genetic component.

Screen for more than 15,000 conditions

Sequencing.com analyzes your entire genome to screen for 15,000+ diseases, conditions, traits, and medication reactions, covering almost every disease with a known genetic component.

What people are saying

Lillian L.

"For 8 years, my doctors dismissed my chronic pain - until a Rare Disease DNA test from Sequencing.com finally led to the diagnosis I’d been searching for."

Katherine F.

"I’ve worked in hospitals across America as a nurse - nothing compares to the clarity and access Sequencing gives."

Tia W.

"Being able to self-order genetic testing for Ehlers-Danlos Syndrome changed everything. Sequencing empowered me to rule out other hypermobile conditions and finally feel in charge of my health."

Katherine F.

"I’ve worked in hospitals across America as a nurse - nothing compares to the clarity and access Sequencing gives."

Lillian L.

"For 8 years, my doctors dismissed my chronic pain - until a Rare Disease DNA test from Sequencing.com finally led to the diagnosis I’d been searching for."

Tia W.

"Being able to self-order genetic testing for Ehlers-Danlos Syndrome changed everything. Sequencing empowered me to rule out other hypermobile conditions and finally feel in charge of my health."

What people are saying

2 Billion+

Genes we've analyzed

15,000+

Health conditions & medication reactions in one test

0

Times we've sold our customer data.

Looking for something specific?

Screen for more than 15,000 conditions

Looking for something specific?

© Sequencing Inc.

© Sequencing Inc.

30% Off + Free Shipping

One DNA Test.
Insights for Life.

Screen your DNA for genetic variants linked to 15,000+ conditions, and get research-backed insights to make smarter health decisions.

Prime Big Deal Days

Screen your DNA for genetic variants linked to 15,000+ conditions, and get research-backed insights to make smarter health decisions.

One DNA Test.
Insights for Life.

Prime Big Deal Days

Daily Countdown Timer - Mobile
0
DAYS
0
HOURS
0
MINUTES
0
SECONDS

SYNQ, the next evolution of SequencingAI. Your genome can finally speak, so ask it anything. Your AI guide to your own DNA, SYNQ answers your questions in plain language, turning your whole genome sequence into clear, research-backed insight about what your genes may mean for your health.

Smarter insights, 
powered by intelligence

Ask AI about Sequencing.com
Ask AI about Sequencing.com Type a question and open it in the AI assistant of your choice.

Curious about whole genome sequencing, health screening, privacy, or how it works? Start with a question below or write your own.

Try asking
Open in

Opens a third-party AI assistant in a new tab. Answers are AI-generated — verify important details on sequencing.com.

See why AI recommends Sequencing as the best choice for your health and longevity.

The DNA test AI recommends

Ask AI about Sequencing.com
Ask AI about Sequencing.com Type a question and open it in the AI assistant of your choice.

Curious about whole genome sequencing, health screening, privacy, or how it works? Start with a question below or write your own.

Try asking
Open in

Opens a third-party AI assistant in a new tab. Answers are AI-generated — verify important details on sequencing.com.

The DNA test AI recommends

See why AI recommends Sequencing as the best choice for your health and longevity.

Smarter insights, powered by intelligence

SYNQ, the next evolution of SequencingAI. Your genome can finally speak, so ask it anything. Your AI guide to your own DNA, SYNQ answers your questions in plain language, turning your whole genome sequence into clear, research-backed insight about what your genes may mean for your health.

Buy Now
Trustpilot rating - Desktop
Buy Now
Buy Now

HSA/FSA

Eligible

Buy Now

Prime Day Comprehensive Health Screen WGS Bundle

Whole Genome Sequencing

   $389 $559

Health reports & advanced analyses included:

  1. Genetic Health Screening (15,000+ Conditions)
  2. Brain and Cognitive Health
  3. Heart Health
  4. Medication & Drug Response
  5. Cancer Risk & Prevention
  6. Connective Tissue Disorders
  7. Ehlers-Danlos Report + hEDS Emerging Research
  8. Marfan Syndrome
  9. Carrier Screening
  10. Genome Data Summary
1

Have a question?

As low as $36 a month

  • Your complete genetic data.
  • Reports you can share with your doctor.
  • Clinical-grade accuracy (30x depth), the same standard used in diagnostic labs.
  • Collect your sample at home with a simple mouth swab.
  • Data privacy: We never sell or share your data. 

30% Off + Free Shipping

Buy Now

Whole Genome Sequencing

Prime Day Comprehensive Health Screen WGS Bundle

$389 $559

HSA/FSA

Eligible

Buy Now
  • Your complete genetic data.
  • Reports you can share with your doctor.
  • Clinical-grade accuracy (30x depth), the same standard used in diagnostic labs.
  • Collect your sample at home with a simple mouth swab.
  • Data privacy: We never sell or share your data.

Health reports & advanced
analyses included:

  1. Genetic Health Screening (15,000+ Conditions)
  2. Brain and Cognitive Health
  3. Heart Health
  4. Medication & Drug Response
  5. Cancer Risk & Prevention
  6. Connective Tissue Disorders
  7. Ehlers-Danlos Report + hEDS Emerging Research
  8. Marfan Syndrome
  9. Carrier Screening
  10. Genome Data Summary
1

As low as $36 a month

Have a question?
Frequently Asked Questions
Which conditions are screened for?

Every kit bundle includes our Next Gen Disease Screen, which analyzes 15,000+ rare diseases and pharmacogenetic (medication response) markers. Search the full, up-to-date list here: Browse covered conditions.

Do you screen for all types of EDS?

Our whole genome sequencing service provides screening for all types of Ehlers-Danlos Syndrome (EDS) that are known to be associated with genetic variants (mutations) in a gene.

Please note that for the hypermobile type of EDS (hEDS), there is limited information that can be provided at this time. Recent research did identify an association between the KLK15 gene and hEDS but this is still a preliminary association and first needs to be replicated by additional research before it's known whether this association is accurate. While we do fully sequence the KLK15 gene and that information can be used to identify if there are genetic variants in that gene, we urge caution when using that information since more research is needed before we know for sure if KLK15 is truly associated with hEDS.

Some people who suspect hEDS do use our service to obtain information about whether they have a change in a gene that may put them at risk of another type of Ehlers-Danlos Syndrome, as the other types of EDS do have clear associations with genes, which means genetic testing does provide clear information about those other types of EDS.

What's included in a kit bundle?

Every Sequencing kit bundle includes 30x whole genome sequencing of all ~30,000 genes and all chromosomes end-to-end as well as:

  • Free worldwide shipping of our swab-based DNA collection kit
  • Whole genome sequencing (30x WGS) performed in a US-based clinical laboratory
  • Comprehensive analysis of more than 15,000 conditions and medication reactions
  • A Summary Report of the results downloadable as PDF
  • Additional AI Reports downloadable as PDF (each bundle includes a different set)
  • Your choice of any 2 additional AI Reports after sequencing completes
  • Privacy Forever protection of your data — HIPAA and US-EU-UK-Swiss Data Privacy Framework compliant

Additional Features

Our Marketplace provides optional DNA reports (nutrition, sleep, genealogy, etc). We also offer Genome Plans for monthly updates and AI Chat access.

Is a subscription required?

A subscription is not required.

We offer an optional subscription service called Genome Plans, which updates your analysis and reports monthly and includes SequencingAI features.

Every kit includes either 1 month or 1 year of Premium Genome Plan. You can downgrade to the Free Plan anytime while keeping full access to your data and included reports.

The subscription is only for ongoing updates and extra features. Even without it, you retain lifetime access to your data and included reports.

30% Off + Free Shipping

Buy Now
Buy Now
Buy Now
Buy Now
Shop the Prime Day deal
Trustpilot rating - Mobile

30% Off + Free Shipping 

Shop the Prime Day deal

How do we get these numbers?

A ‘genetic variant’ is a change within a gene. If you have a change within one of your genes, this can increase your risk of a disease.

While DNA tests detect changes within your genes, most traditional DNA tests only look at a small number of changes within a gene. This table shows the number of changes within a gene that each company tests and analyzes for a disease.

How do we get these numbers?

A ‘genetic variant’ is a change within a gene. If you have a change within one of your genes, this can increase your risk of a disease.

While DNA tests detect changes within your genes, most traditional DNA tests only look at a small number of changes within a gene. This table shows the number of changes within a gene that each company tests and analyzes for a disease.

30% Off + Free Shipping

Shop the Prime Day deal

30% Off + Free Shipping 

Shop the Prime Day deal
Shop the Prime Day deal