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Celebrate DNA Day With Whole Genome Sequencing

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How do we get these numbers?

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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 Most Comprehensive Rare Disease Screening

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Made Possible With Whole Genome Sequencing

DNA tests from 23andMe, AncestryDNA, and most other companies use older technology that produces data on a very small subset of the total genome.
 
Whole genome sequencing is an entirely different class of technology that tests every letter of your DNA, including all ~30,000 genes and all chromosomes end-to-end.

0.1%

100%

Of Your Genome

Of Your Genome

Made Possible With Whole Genome Sequencing

DNA tests from 23andMe, AncestryDNA, and most other companies use older technology that produces data on a very small subset of the total genome.
 
Whole genome sequencing is an entirely different class of technology that tests every letter of your DNA, including all ~30,000 genes and all chromosomes end-to-end.

0.1%

100%

Of Your Genome

Of Your Genome

Ready To Get Sequenced?

Start by ordering the world’s most comprehensive DNA test kit.

Ready To Get Sequenced?

Start by ordering the world’s most comprehensive DNA test kit.

Obtains data on around 3 billion positions within your genome (100% of your genome). Also includes the ability to download your raw genome data files for no additional fee. This includes FASTQ, BAM and VCFs covering all genetic variations: Single Nucleotide Polymorphisms (SNPs), Insertions and Deletions (INDELs), Structural Variations (SVs), Copy Number Variations (CNVs) and Mitochondrial Heteroplasmy (MITO).

DNA Day WGS Health Screen Bundle

$399 $1,150

HEALTH AREAS INCLUDED:

Full Access To All Raw Genome Data & Analyzed Data:


3 billion genetic variants

All 30,000 genes sequenced

All chromosomes fully sequenced incl. the mitochondrial & Y chromosomes

100% of your genome

30x genome sequencing

Whole Genome Sequencing

One Month Premium Genome Plan

Add To Cart

As Low As $37/Month 

  1. Rare Disease Screening
    (15,000+ Conditions + EDS)
  2. Carrier Screening
  3. Connective Tissue Disorders
  4. Autoimmune Disorders
  5. Developmental Disorders
  6. Cardiovascular Health
  7. Brain Health
  8. Medication & Drug Response
  9. Reproductive & Hormonal Health
  10. Cancer Risk
  11. Skin Health
  12. Neurological Health

Bonus Report

Ancestry Explorer

DNA Day WGS Health Screen Bundle

$399
$1,150

One Month Premium Genome Plan

Whole Genome Sequencing

Full Access To All Raw Genome Data & Analyzed Data:

3 billion genetic variants

All 30,000 genes sequenced

All chromosomes fully sequenced including the mitochondrial & Y chromosomes

100% of your genome

30x genome sequencing depth

HEALTH AREAS INCLUDED:

  1. Rare Disease Screening (15,000+ Conditions + EDS)
  2. Carrier Screening
  3. Connective Tissue Disorders
  4. Autoimmune Disorders
  5. Developmental Disorders
  6. Cardiovascular Health
  7. Brain Health
  8. Medication & Drug Response
  9. Reproductive & Hormonal Health
  10. Cancer Risk
  11. Skin Health
  12. Neurological Health

Bonus Report

Ancestry Explorer

As Low As $37/Month 

or

OR

Obtains data on around 3 billion positions within your genome (100% of your genome). Also includes the ability to download your raw genome data files for no additional fee. This includes FASTQ, BAM and VCFs covering all genetic variations: Single Nucleotide Polymorphisms (SNPs), Insertions and Deletions (INDELs), Structural Variations (SVs), Copy Number Variations (CNVs) and Mitochondrial Heteroplasmy (MITO).

Rare Disease List

World's Most Comprehensive Rare Disease Screening

Rare Disease ListAdd To CartAdd To Cart

Celebrate DNA Day With Whole Genome Sequencing

No Insurance Companies

Keep Your Results Anonymous

Save Thousands Without  A Doctor's Lab Order

Privacy By Going Direct

Working directly with CLIA-certified labs for clinical-grade 30x Sequencing.

Meet The Families In Need

In honor of Rare Disease Day, we invite you to be part of a special initiative:
For every 50 Rare Disease Day WGS Special Bundles ordered, we pledge to donate a bundle to a family grappling with unresolved health mysteries. These families in need stand to gain invaluable insights from genome sequencing, offering them a beacon of hope in their search for answers.

Valerie

Madyn

Jonathan

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—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.

Meet The Families In Need

In honor of Rare Disease Day, we invite you to be part of a special initiative:
For every 50 Rare Disease Day WGS Special Bundles ordered, we pledge to donate a bundle to a family grappling with unresolved health mysteries. These families in need stand to gain invaluable insights from genome sequencing, offering them a beacon of hope in their search for answers.

Valerie

View Story

Madyn

View Story

Jonathan

View Story

From Our Founder’s Heart: Dr. Brandon Colby's Story

Start Your Journey with Next-Gen Disease Screen

Traditional labs charge thousands of dollars to test for a single disease, and at most, up to 30 diseases. These expensive tests often only scratch the surface of your genes, leaving a wealth of crucial information untouched.

NGDS is here to change that narrative. Analyzing whole genome sequencing data, NGDS provides a straightforward assessment of your genetic risk for more than 15,000 diseases, conditions, traits, and medication reactions. This transformative tool enables you to screen your entire genome for almost every disease with a known genetic component.

View List Of Rare Diseases

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.

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

Start Your Journey with Next-Gen Disease Screen

Traditional labs charge thousands of dollars to test for a single disease, and at most, up to 30 diseases. These expensive tests often only scratch the surface of your genes, leaving a wealth of crucial information untouched.

View List Of Rare Diseases

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

Ginny

Inga

View Story

Andrew

Kenzie

Andrew

View Story

Kenzie

View Story

Alyssa

View Story

Meet The Families In Need

In honor of Rare Disease Day, we invite you to be part of a special initiative:
For every 50 Rare Disease Day WGS Special Bundles ordered, we pledge to donate a bundle to a family grappling with unresolved health mysteries. These families in need stand to gain invaluable insights from genome sequencing, offering them a beacon of hope in their search for answers.

Valerie

Madyn

Jonathan

Ginny

Andrew

Kenzie

Alyssa

Meet The Families In Need

In honor of Rare Disease Day, we invite you to be part of a special initiative:
For every 50 Rare Disease Day WGS Special Bundles ordered, we pledge to donate a bundle to a family grappling with unresolved health mysteries. These families in need stand to gain invaluable insights from genome sequencing, offering them a beacon of hope in their search for answers.

Valerie

View Story

Madyn

View Story

Jonathan

View Story

Inga

View Story

Andrew

View Story

Kenzie

View Story

Made Possible With Whole Genome Sequencing

DNA tests from 23andMe, AncestryDNA, and most other companies use older technology that produces data on a very small subset of the total genome.
 
Whole genome sequencing is an entirely different class of technology that tests every letter of your DNA, including all ~30,000 genes and all chromosomes end-to-end.

0.1%

100%

Of Your Genome

Of Your Genome

Order Special Sequencing BundleOrder Special Sequencing Bundle

Free Shipping

HSA/FSA Eligible

+

Free Shipping + HSA/FSA Eligible

Alyssa

Order Special Sequencing Bundle

Unlock your DNA’s full potential with our DNA Day Special Bundle. Get insights into 12 health areas and dive deeper into your genome with SequencingAI.

Includes 12 Health Reports + 1 Bonus Ancestry Report

© 2025 Sequencing.com

Includes 12 Health Reports + 1 Bonus Ancestry Report

© 2025 Sequencing.com

Unlock your DNA’s full potential with our DNA Day Special Bundle. Get insights into 12 health areas and dive deeper into your genome with SequencingAI.