HEREDITARY RISK
It runs in your family. Now you can know if it runs in your genes.
Many serious conditions — from cancer to cardiac disease — have a genetic basis that can be identified before symptoms appear. Whole genome sequencing screens your complete DNA for hereditary variants across hundreds of conditions, giving you and your physician actionable insight.
Condition Coverage
One test. Five critical categories.
Our whole genome test analyses variants across the major hereditary risk categories — no need for separate panels.
Cardiovascular
26 reports
Conditions involving the heart, blood vessels (arteries, veins), and the body's circulatory system.
- Aortic Aneurysm
- Arrhythmogenic Cardiomyopathy
- Brugada Syndrome
- Catecholaminergic Polymorphic Ventricular Tachycardia
Cancer
33 reports
Diseases characterized by the uncontrolled growth and spread of abnormal cells; also known as oncological conditions.
- BAP1 Tumour Predisposition Syndrome
- Birt-Hogg-Dubé Syndrome
- Breast and Ovarian Cancer Genes Beyond BRCA1/2
- CYLD Cutaneous Syndrome
Neurological
59 reports
Conditions affecting the brain, spinal cord, and the network of nerves that control the body.
- Adult-Onset Leukodystrophies (CSF1R, LMNB1, Nasu-Hakola)
- Aicardi-Goutieres Syndrome
- Alexander Disease
- Alzheimer disease
Musculoskeletal
31 reports
Disorders involving the bones, joints, ligaments, tendons, and muscles, affecting movement and the body's structure.
All musculoskeletal reports →Metabolic
67 reports
Conditions impacting the body's chemical processes for converting food into energy, building tissues, and eliminating waste.
- Acid Sphingomyelinase Deficiency (Niemann-Pick Disease Types A and B)
- Alkaptonuria
- Alpha-Mannosidosis and Other Glycoproteinoses
- BH4 Deficiency & Monoamine Neurotransmitter Disorders
Whole genome coverage
Variants identified per test
Customized clinical reports
Sequencing accuracy
Family Impact
One result, every relative.
A hereditary finding doesn't just apply to you. When your genome reveals a pathogenic variant, every first-degree relative — parents, siblings, children — has up to a 50% chance of carrying the same variant.
That single data point can guide targeted screening, earlier surveillance, or preventive intervention for your entire family. One test can protect a generation.
You
Pathogenic variant identified
Siblings & Parents
50% probability — targeted testing recommended
Children
50% probability — early surveillance enabled
Extended Family
Cascade screening can reach 2nd & 3rd degree relatives
The Process
Four steps to get started. No clinic visit required.
Order your kit
Free delivery worldwide.
Collect your sample
Simple finger-prick blood spot collection at home. Takes 5 minutes. Everything you need is in the kit.
Send it back
Pre-paid return label included. Drop it in any post box.
Access your results
Reports delivered to your Genome Manager in 6–8 weeks. Review every finding and share directly with your physician.
Know what runs in your genes
One kit, sent to your home. Your entire genome sequenced at the clinical standard used for diagnostic decisions. 470+ physician-ready reports with Premium, delivered to your Genome Manager in 6–8 weeks — permanent and updated as science advances.
Free shipping · Results in 6–8 weeks
