All Panels Package

$499.00 $199.00 Save 60%

List of Reports included :

Achromatopsia Panel
ACMG Panel
Acrodermatitis Enteropathica Panel
Acute Hepatic Porphyria Report
Afibrinogenemia Panel
Aicardi-Goutières Syndrome Panel
Alagille Syndrome Panel
Alkaline Phosphatase Panel
Alport Syndrome Panel
Amyloidogenic transthyretin amyloidosis Panel
Aneurysm risk Panel
Aortic Aneurysm Panel
Asthma Susceptibility Panel
Autism and Neurodevelopmental Disorders Panel
Autism Panel
Autoimmunity Panel
Autoinflammatory Panel
Autophagy Panel
Bardet Biedl Syndrome Panel
Bartter and Gitelman's Syndromes Report
Breast Cancer Panel
Brugada Syndrome Panel
Cardiometabolic Disorders Panel
Cardiomyopathies Panel
Cardiovascular Panel
Carrier Screening Panel
Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) Panel
Cerebral Amyloid Angiopathy Report
Cerebral cavernous malformations Panel
Charcot-Marie-Tooth Disease Panel
Chédiak-Higashi Syndrome Panel
Chronic Granulomatous Disease Panel
Chronic Traumatic Encephalopathy Panel
Ciliopathies Panel
Circadian Panel
COL7A1 Panel
Combined Pituitary Hormone Deficiency Panel
Congenital Adrenal Hyperplasia Panel
Congenital Cataracts Panel
Congenital Disorders of Glycosylation Panel
Congenital Myasthenic Syndrome Panel
Congenital Neutropenia Panel
Congenital Sucrase-Isomaltase Deficiency Panel
Connective Tissue Panel
Copper Metabolism Disorders Panel
Cowden Syndrome Panel
Crohn Disease Panel
Cutis Laxa Panel
Cystic Fibrosis Panel
Cystinuria Panel
Dentist Panel
Dermatology Panel
Diabetes Panel
Diamond-Blackfan Anemia Panel
Dilated Cardiomyopathy Panel
Distal Myopathies Panel
Dyskeratosis Congenita Panel
Dystonia, Myotonia and Paroxysmal Dyskinesia Report
Ectodermal Dysplasias Panel
Ectopia Lentis Panel
Ehlers-Danlos Syndrome Panel
Endocrinology Panel
Epidermolysis Bullosa Panel
Epilepsy Panel
Erythropoietin Receptor Report
Fallot's Tetralogy Panel
Familial Hypercholesterolemia Panel
Familial Intrahepatic Cholestasi Panel
Fanconi Anemia Panel
Female infertility Panel
Focal Segmental Glomerulosclerosis and Complement Genetic Study Report
Frontotemporal Dementia Panel
Gastroenterology Panel
Gilbert Syndrome Panel
Glaucoma Panel
Glucocorticoid Deficiency Panel
Glycogen Storage Diseases
Graves' Disease Panel
Hearing Loss and Deafness Panel
Hematology Panel
Hemiplegic Migraine Panel
Hemochromatosis Panel
Hemolytic Uremic Syndrome and Autosomal Dominant Interstitial Nephritis Reports
Hereditary Amyloidosis Panel
Hereditary Cancer Panel
Hereditary Colorectal Cancers Panel
Hereditary Hemorrhagic Telangiectasia Panel
Hereditary Kidney Cancers Report
Hereditary Myopathies Panel
Hereditary Optic Neuropathy Panel
Hereditary Pancreatitis Panel
Hereditary Prostate Cancer Report
Hereditary Spastic Paraplegia (HSP) Panel
Hereditary Vitreoretinopathy Panel
Hermansky-Pudlak syndrome Panel
Hyper IgE syndromes Panel
Hypertrophic Cardiomyopathy Panel
Hypothyroidism Panel
Idiopathic short stature Panel
Inflammatory Bowel Disease Panel
Joubert and Meckel-Gruber syndromes Panel
Leigh Syndrome Panel
Leukodystrophy Panel
Long QT Syndrome Panel
Lysosomal Storage Disorders Panel
Male infertility Panel
Marfan Syndrome Panel
McArdle Disease Report
Metabolic Panel
Methylation Mechanisms Panel
MODY Panel
Multiple Sclerosis Panel
Nephrology Panel
Neurofibromatosis Panel
Neurology Panel
Neuronal Ceroid Lipofuscinosis Panel
Non-syndromic Retinitis Pigmentosa Panel
Noonan Syndrome Panel
Nuclear Mitochondrial Genes Panel
Obesity Panel
Obstructive Hypertrophic Cardiomyopathy Panel
Oncology Panel
Ophthalmology Panel
Osteoarthritis and rare cartilage diseases Panel
Osteogenesis Imperfecta Panel
Osteopetrosis Panel
Oxidative Stress Panel
Palb2 Panel
Parkinson - Alzheimer - Dementia Panel
Parkinson's Disease Panel
Pediatric Panel
Pendred Syndrome Panel
Periodic Paralysis Panel
Polycystic Kidney Disease Panel
Polycystic Ovary Syndrome Panel
Porphyria Panel
Premature Ventricular Contractions Panel
Primary Ciliary Dyskinesia Panel
Primary Immunodeficiency Report
Pulmonary Arterial Hypertension
Pulmonary Surfactant Dysfunctions Panel
Pulmunology Panel
RASopathies Panel
Recurrent pregnancy loss Panel
Red Blood Cell Membrane Disorders Panel
Rheumatoid Arthritis Panel
Schizophrenia Panel
Seckel Syndrome Panel
Secondary Hypogonadism Panel
Sensory Panel
Serotonin Metabolism Deficiency Panel
Short QT Syndrome Panel
Sjögren’s Syndrome Panel
Skeletal and Connective Tissue Disorders Panel
Skeletal Dysplasias Panel
Systemic lupus erythematosus Panel
Systemic mastocytosis Panel
Type 4 Spastic Paraplegia Report
Tyrosinemia Panel
Ulcerative Colitis Panel
Urea cycle disorder Panel
Valosin-Containing Protein Panel
Vascular Dementia Panel
Very long chain acyl-CoA dehydrogenase deficiency Panel
Von Willebrand Panel
Waardenburg Syndrome Panel
WEST Syndrome Panel
Wilson Disease Panel

  • Available in less than 24 hours
  • Based on Whole Genome Sequencing
  • Investigates SNP and Indel mutations up to 150 bp


How will my data be used?

Your data is yours. Which is why we have developed proprietary software linked to a dedicated platform, the Genome Manager, to provide you with unique access to your data whenever you want, wherever you are.

How can my doctor use the results?

You will be provided with a digital version of the raw data and reports. Thanks to these in-depth tools, you will be able to share your preferred information with your geneticist and/or doctor to indicate and plan the healthiest course for you. 

How will I receive my reports?

The first thing to do when you receive your kit is to register it on your Genome Manager account. Dante's proprietary platform will keep you up-to-date on all stages of your genetic journey, providing you with the real-time status of your sample and where you can download your free report and raw data* at any time.

*Raw data will be available free of charge for the first 30 days after release.

How can I add other reports to my account?

At any time, you can log into your Genome Manager account and visit the Shop section. Here you will find a catalog with more than 150 additional reports dedicated to all areas of health. In addition, by subscribing to our newsletter you can always see new reports and panel updates.

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