Gene | Condition | # of Genetic Variants Analyzed | |
---|---|---|---|
BRCA 1/2 | Breast, Ovarian, Other Cancers | 23,975 | 3 |
KCNQ1 | Preventable Sudden Death, SIDS | 4,677 | 0 |
CFTR | Cystic Fibrosis | 2,716 | 28 |
RYR1 | Preventable Reaction to Anesthesia | 3,839 | 0 |
Our whole genome sequencing obtains information on your entire genome of more than 3 billion genetic variants.
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100% of your DNA data is vital for evaluating your genetic risk for diseases and adverse reactions to medical treatments.
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Receive personalized health guidance now and throughout your life, and learn about potential risk of diseases and conditions.
Whole genome sequencing is the only DNA test that obtains 100% of your genome. Once you have sequenced yourself, the data that's obtained will provide insights that help protect your health throughout your life.
Even if new genes are discovered in the future, you won't need to take another DNA test. We will simply reanalyze the data we’ve already obtained to provide you with insights about these new discoveries.
Deciphering the human genome was not easy. Sequencing the first whole genome, which was completed in 2003, took 13 years and cost $3 billion dollars.
The information from the Human Genome Project has allowed us to better diagnose disease, detect certain diseases earlier, and make life-saving improvements in preventive medicine.
Thanks to rapid technological advancements over the last 20 years, the cost of whole genome sequencing is now within reach for virtually all people who want to have better control of their health and wellness.
Anyone can use the information from our affordable sequencing service for their own personal edification. Health professionals also use it to help them gain more insight into their patients’ conditions in order to improve outcomes.
Become empowered to take action and make positive changes to your life when you receive health guidance that’s based on their DNA. Our service provides more information about your DNA than any other type of genetic testing.
LIMITED TIME DNA DAY SPECIAL SALE
DNA Day Rare Disease Special WGS Bundle
$1,150
$399
+ Free Shipping
We don’t sell your data to anyone.
Bundle Includes
Accepted Payment Methods
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).
Start with our Rare Disease Month Special WGS Bundle, or explore a range of tailored bundles designed to provide insights across key health areas. Discover the bundle that’s right for you!
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