PROACTIVE HEALTH
You feel fine today. Your genome can tell you what to watch for tomorrow.
Most hereditary conditions are manageable when caught early — but they rarely show symptoms until damage is underway. Whole genome sequencing maps your complete genetic risk profile so you and your physician can plan ahead, not react after the fact.
Coverage Overview
470+ clinical reports across the conditions that matter most.
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
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
Hematological
25 reports
Conditions affecting the blood, blood-forming organs (like bone marrow), and blood components such as cells and plasma.
- Congenital Afibrinogenemia
- Congenital Dyserythropoietic Anaemias
- Congenital Thrombotic Thrombocytopenic Purpura
- Diamond-Blackfan Anemia
Immunological
34 reports
Disorders of the immune system, including allergies, autoimmune diseases, and immunodeficiencies.
- Activated PI3K-Delta Syndrome (APDS)
- Agammaglobulinaemia (XLA and Autosomal Forms)
- Ataxia-Telangiectasia
- Autoimmune Disease
Patient Outcomes
Real answers that changed lives.
RARE GENETIC SYNDROME
Two conditions from a single test
Years of specialist referrals found nothing. A single whole genome test identified Noonan Syndrome and RUNX1 deficiency, both accepted by NHS genetics.
Data accepted by NHS genetics at Queen Elizabeth University Hospital Glasgow. Clinical action taken by the NHS team. Dante produced the genomic data. This is a documented outcome at a named institution, not an endorsement by NHS.
CHILDHOOD EPILEPSY
A dietary intervention that changed everything
A 4-year-old with uncontrolled seizures. Genomic sequencing identified GLUT-1 Deficiency, shifting treatment from anticonvulsants to a ketogenic diet.
Identification of the metabolic basis allowed dietary intervention. All clinical decisions were made by the treating physicians.
BREAST CANCER
Genomic data that arrived before the diagnosis
Genome sequenced in 2019. Breast cancer diagnosed in 2021. Pre-existing pharmacogenomic data flagged a drug incompatibility before treatment began.
Pre-existing genomic data informed the treatment decision. The oncology team made the final clinical choice.
Why Whole Genome
The case for knowing everything.
Complete coverage, not a pre-selected panel
Targeted panels test a handful of genes chosen in advance. Whole genome sequencing reads all 6 billion base pairs — giving your physician a complete dataset to work from, now and in the future.
Actionable before symptoms appear
Many hereditary conditions are highly manageable when caught early. Knowing your risk profile lets you and your physician build a monitoring plan based on your actual biology.
Sequenced once, re-analysed for life
Your genome data is stored permanently. As new gene-disease associations are validated, your reports update automatically — no repeat testing required.
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.
One test. A lifetime of answers.
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
