Our Rare Disease Special Offer Is Back!
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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 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.
Whole Genome Sequencing
Rare Disease Bundle
$399 $639
Privacy First Data Protection
We don’t sell or share your data with anyone.
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 Special
WGS Bundle
$399 $2,719
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
Free Upgrade: Expedited Processing
- Healthcare Professional
(Limited Time Special Report) - Rare Disease Screening
(15,000+ Conditions + EDS) - Carrier Screening
- Cancer Risk
- Autoimmune Disorders
- Cardiovascular Health
- Neurological Health
- Endocrine Health
Rare Disease Special WGS Bundle
$399 $2,719
HEALTH AREAS INCLUDED:
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
- Healthcare Professional
(Limited Time Special Report) - Rare Disease Screening (15,000+ Conditions + EDS)
- Carrier Screening
- Cancer Risk
- Autoimmune Disorders
- Cardiovascular Health
- Neurological Health
- Endocrine Health
Free Expedited Processing ($1300 Value)
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).
World's Most Comprehensive Rare Disease Screening
Rare Disease Special Offer Is Back!
We are dedicated to helping you solve your medical mysteries with our Rare Disease Month Special Bundle. Get insights into 8 health areas and dive deeper into your DNA with SequencingAI.
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.
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.
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.
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.
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
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.
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.
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
Free Shipping
HSA/FSA Eligible
+
Free Shipping + HSA/FSA Eligible
We are dedicated to helping you solve your medical mysteries with our Rare Disease Month Special Bundle. Get insights into 8 health areas and help sponsor free genetic testing for families in need.
8 Health Reports Included + Free Upgraded To Expedited Procesing ($1,300 Value)
Our Tests Vs Our Competitors
23andMe is a registered trademark of 23andMe, Inc., AncestryDNA is a registered trademark of Ancestry Operations Inc. dba Ancestry, Family Tree DNA is a registered trademark of Gene By Gene, Ltd., MyHeritage is a registered trademark of MyHeritage Ltd., Dante Labs is a registered trademark of Dante Labs, Inc., Nebula Genomics is a registered trademark of Nebula Genomics, Inc., HomeDNA is a trademark of DNA Diagnostic Center, Inc., Living DNA is a registered trademark of Living DNA Ltd., Vitagene is a registered trademark of Vitagene, 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., Ancestry Operations Inc. dba Ancestry, Gene By Gene, Ltd., MyHeritage Ltd., Dante Labs, Inc., Nebula Genomics, Inc., DNA Diagnostic Center, Inc., Living DNA Ltd., or Vitagene, Inc.
© 2025 Sequencing.com
Our Tests Vs Our Competitors
23andMe is a registered trademark of 23andMe, Inc., AncestryDNA is a registered trademark of Ancestry Operations Inc. dba Ancestry, Family Tree DNA is a registered trademark of Gene By Gene, Ltd., MyHeritage is a registered trademark of MyHeritage Ltd., Dante Labs is a registered trademark of Dante Labs, Inc., Nebula Genomics is a registered trademark of Nebula Genomics, Inc., HomeDNA is a trademark of DNA Diagnostic Center, Inc., Living DNA is a registered trademark of Living DNA Ltd., Vitagene is a registered trademark of Vitagene, 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., Ancestry Operations Inc. dba Ancestry, Gene By Gene, Ltd., MyHeritage Ltd., Dante Labs, Inc., Nebula Genomics, Inc., DNA Diagnostic Center, Inc., Living DNA Ltd., or Vitagene, Inc.
© 2025 Sequencing.com
8 Health Reports Included + Free Upgraded To Expedited Procesing ($1,300 Value)
Every Purchase Helps A Family In Need
In honor of Rare Disease Month, Sequencing will donate free genome sequencing to families in need—every purchase in February helps provide free sequencing to those who need it most.
4.4
Valerie
For years, Valerie faced debilitating pain and mobility issues, without answers. Genetic testing was out of reach until she discovered Sequencing.com’s Rare Disease Day program, which led to her diagnosis of Dopa-responsive dystonia. With the right treatment, she’s regained mobility, returned to para sports, and finally found clarity.
Meet:
"This test changed my life. Without it, I’d still be in pain, searching for answers."
Every Purchase Helps A Family In Need
In honor of Rare Disease Month, Sequencing will donate free genome sequencing to families in need—every purchase in February helps provide free sequencing to those who need it most.
Meet:
Valerie
For years, Valerie faced debilitating pain and mobility issues, without answers. Genetic testing was out of reach until she discovered Sequencing.com’s Rare Disease Day program, which led to her diagnosis of Dopa-responsive dystonia. With the right treatment, she’s regained mobility, returned to para sports, and finally found clarity.
"This test changed my life. Without it, I’d still be in pain, searching for answers."