28% OFF + FREE SHIPPING
30x Whole Genome Sequencing

28% OFF + FREE SHIPPING
30x Whole Genome Sequencing

At-home cheek swab DNA kit

360 comprehensive genetic risk reports
Type 2 diabetes
Carrier screening for 27 hereditary conditions


Longevity & wellness assessments

Vitamin A
Gluten Sensitivity
Genetic genealogy insights

Unlimited access to your genetic data

100% of your genome

0.1% of your genome
Other tests
“DNA is more than a time machine that takes us to the past. It also provides us with knowledge for our future, to help us live healthier lives.”

Yaniv Erlich, PhD
Genetics and data pioneer
Cancer Risk
Cardiovascular & Respiratory
Brain & Neurological
Metabolism & Hormonal Health
Autoimmune & Blood
Nutrition, Vitamins & Minerals
Family Planning
Longevity & Healthy Aging
Sleep, Stress & Energy
Fitness & Sports
Skin Health
Ethnicity & Origins










Whole Genome Sequencing is the most comprehensive method for reading DNA available today. Whole Genome refers to all 3 billion base pairs in human DNA, while 30x refers to the number of times each position on the genome is read. By comparison, standard consumer DNA tests read only about 700,000 base pairs of the human genome. In other words, while the industry standard for genetic genealogy has been to look at select sentences of each person’s DNA “book,” Whole Genome Sequencing reads virtually the entire story. 30x sequencing is the industry standard for medical-grade reports and insights.
