Premium Whole Genome Sequencing (30X)

Premium Whole Genome Sequencing Full DNA Test (30X)

Regular price $599.00 Sale price $299.00

The Rare Disease special pricing is reserved to Rare Disease Patients.

Once you receive our collection kit, create your account on Genome Manager and upload your diagnosis on the "Upload Medical Documents" section in order to qualify your Rare Disease special order.

  • Whole Genome Sequencing 30X (industry standard coverage)
  • Now with a new Rare Disease Report
  • Analysis of 100% of your DNA
  • Raw Data available free of charge (FASTQ, BAM and VCF)
  • Sequenced in our own new European Sequencing Center


Note: the turnaround time starts when the kit is received in our Lab in L'Aquila, Italy

Click here to see how your reports will look like

What reports you get


Design a Personalized Diet based on your Whole Genome with usefull insights on what vitamins and nutrients and food are the best for you

25 Conditions (tap here)

  1. Metabolism
  2. Obesity
  3. Vitamin B2
  4. Vitamin B6
  5. Vitamin B12
  6. Vitamin C
  7. Vitamin D
  8. Vitamin E
  9. Monounsaturated fats intake
  10. Polyunsaturated fats intake
  11. Blood levels of omega-6 and omega-3
  12. Eating between meals
  13. Hunger feeling
  14. Satiety after eating
  15. Dietary disinhibition
  16. Eating desire Sweet food craving
  17. Caffeine metabolism
  18. Sweet taste
  19. Lactose intolerance
  20. Alcohol flush
  21. Post dietary weight regain
  22. Adiponectin levels
  23. Folate


Choose the best training for you based on your whole genome. Discover how your genetic variants impact your fitness, sport activities and performance.

28 Conditions (tap here)

  1. Endurance Workout
  2. Strength Workout
  3. Maximum capacity for oxygen consumption (VO2MAX)
  4. Muscle Strength
  5. Tendinopathy
  6. Physical Activity in Weight Loss
  7. Blood Pressure Response to Physical Activity
  8. HDL (good) Cholesterol Response to Physical Activity
  9. Loss of Body Fat Response to Physical Activity
  10. Insulin Sensitivity Response to Physical Activity
  11. Injury Risk
  12. Sodium
  13. Calcium
  14. Post Exercise Recovery
  15. Cruciate Ligament Rupture
  16. Carpal Tunnel Syndrome
  17. Shoulder Dislocation
  18. Stress Fracture Period Prevalence
  19. Rotator Cuff Disease
  20. Muscle Cramps
  21. Increase of Glucose Uptake in Response to Exercise
  22. Body Mass Index
  23. Osmotic Stress
  24. Exercise-induced Myopathy
  25. Sprint
  26. Potassium Balance (K)
  27. Creatine Kinase
  28. Quadriceps Strength


Learn about predispositions to wellness and lifestyle conditions caused by your genetic variants, get actionable advice and insights to live a healthier life

70 Conditions (tap here)

  1. Andermann Syndrome
  2. Arrhythmogenic Right Ventricular
  3. Cardiomyopathy
  4. Beta Thalassemia
  5. Bloom Syndrome
  6. Brugada Syndrome
  7. Canavan Disease
  8. Catecholaminergic Polymorphic
  9. Ventricular Tachycardia
  10. Cystic Fibrosis
  11. D-Bifunctional Protein Deficiency
  12. Dihydrolipoamide Dehydrogenase
  13. Deficiency
  14. Dilated Cardiomyopathy
  15. Ehlers-Danlos Syndrome
  16. Fabry Disease
  17. Familial Adenomatous Polyposis
  18. Familial Dysautonomia
  19. Familial Hypercholesterolemia
  20. Familial Hyperinsulinism
  21. Familial Hypertrophic Cardiomyopathy
  22. Familial Thoracic Aortic Aneurysm And Dissection
  23. Fanconi Anemia
  24. Gaucher Disease
  25. Glycogen Storage Disease Type I
  26. Gracile Syndrome
  27. Hereditary Fructose Intolerance
  28. Junctional Epidermolysis Bullosa
  29. Juvenile Polyposis Syndrome
  30. Left Ventricular Noncompaction
  31. Leigh Syndrome
  32. Li-Fraumeni Syndrome
  33. Limb-Girdle Muscular Dystrophy
  34. Loeys-Dietz Syndrome
  35. Long Qt Syndrome
  36. Malignant Hyperthermia
  37. Maple Syrup Urine Disease
  38. Marfan Syndrome
  39. Medium-Chain Acyl-Coenzyme A
  40. Dehydrogenase Deficiency
  41. Mucolipidosis Type Iv
  42. Neurofibromatosis Type 2
  43. Neuronal Ceroid Lipofuscinosis Cln1 Related
  44. Neuronal Ceroid Lipofuscinosis Cln5 Related
  45. Niemann-Pick Disease Type A
  46. Nijmegen Breakage Syndrome
  47. Nonsyndromic Hearing Loss And Deafness Gjb2 Related
  48. Ornithine Transcarbamylase Deficiency
  49. Paragangliomas
  50. Pendred Syndrome
  51. Peutz-Jeghers Syndrome
  52. Phenylketonuria
  53. Pilomatrixoma
  54. Pmm2-Congenital Disorder Of Glycosylation
  55. Polycystic Kidney Disease
  56. Pten Hamartoma Tumor Syndrome
  57. Tuberous Sclerosis
  58. Von Hippel-Lindau Syndrome
  59. Wilson Disease
  60. Primary Hyperoxaluria
  61. Rhizomelic Chondrodysplasia Punctata
  62. Sialic Acid Storage Disease
  63. Sickle Cell Disease
  64. Sjögren-Larsson Syndrome
  65. Tay-Sachs Disease
  66. Tyrosinemia
  67. Usher Syndrome Type I
  68. Zellweger Spectrum Disorder
  69. Age-Related Macular Degeneration
  70. Hereditary Hemochromatosis
  71. Factor V Leiden Thrombophilia
  72. Prothrombin Thrombophilia
  73. Alpha-1 Antitrypsin Deficiency
  74. Glucose-6-Phosphate Dehydrogenase Deficiency

How it works