Foresight Health® Dog

£125.00

The results of DNA testing with Foresight Health are accepted by The Kennel Club

Please note this product is in the process of being phased out. Please search for your breed in the box at the top of the page to find your breed-specific package (we are adding breed packages regularly). 

Our proprietary next-generation testing method tests each mutation thousands of times to ensure accuracy while making DNA testing more affordable than ever.


  • If you want to check which inherited diseases in Foresight Health are applicable to your breed, please use the search bar to find the DNA testing guide for your breed. 
  • Foresight Health covers the DNA tests currently required for breed testing schemes offered by the Kennel Club (search for your breed to find out more).
  • We want to make sure your DNA testing experience is simple yet high quality. The expert geneticists who developed our advanced DNA tests are available for any questions you may have.

How long does it take?

We aim to turn around Foresight Health samples in 15 working days from when the swab arrives back at the lab. However, this is a guideline turnaround and while it can sometimes be a few days quicker, it can also be a few days slower, depending on how busy the lab is.  Our next-generation testing methods take a little longer than the older methods used by other labs but we believe that good things are worth waiting for.

What happens when I order?

We will send you out one of our eco-friendly (and totally recyclable) kits for swabbing your dog's cheek to collect DNA. You activate your kit on our website and send the swab back to us. We begin testing your dog's DNA and you'll be kept updated by our online system and by email as the testing progresses. Once your results are ready you'll be able to see them in a fantastic interactive report on our dedicated results site. 

  • Coagulation Factor VII deficiency (F7)
  • Phosphofructokinase deficiency (PFKD)
  • Coagulation Factor VIII Deficiency (Haemophilia A)
  • Canine Leucocyte Adhesion Deficiency Type I (CLAD)
  • Malignant Histiocytosis
  • Prekallikrein deficiency (KTK)
  • Pyruvate kinase deficiency (PKDef)
  • Arrythmogenic Right Ventricular Cardiomyopathy (ARVC)
  • Glanzmann's Thrombasthenia Type I
  • Congenital Macrothrombocytopaniea
  • Thrombopathia
  • Von Willebrand disease I (vWD1)
  • Von Willebrand disease II (vWD2)
  • Von Willebrand disease III (vWD3)
  • Canine Scott Syndrome
  • Trapped Neutrophil Syndrome (TNS)
  • Coagulopathy P2RY12-related
  • May-Hegglin anomaly
  • Methemoglobinaemia
  • Amelogenesis Imperfecta (AI)
  • Dental hypomineralisation
  • Malignant hyperthermia (MH)
  • Achromatopsia (Cone Degeneration, originally discovered in Alaskan Malamute)
  • Achromatopsia (Cone Degeneration, Hemeralopia, originally discovered in the German Shorthaired Pointer)
  • Achromatopsia 2
  • Bardet-Biedle syndrome 4 (PRA in Puli)
  • Canine Multifocal Retinopathy 1 (CMR1)
  • Canine Multifocal Retinopathy 2 (CMR2)
  • Canine Multifocal Retinopathy 3 (CMR3)
  • Ichthyosis
  • Juvenile Hereditary Cataracts (JHC, Early onset Cataracts)
  • Macular corneal dystrophy
  • Microphthalmia
  • Primary Lens Luxation (PLL)
  • Primary Open Angle Glaucoma (POAG, originally discovered in Beagle)
  • Primary Open Angle Glaucoma (POAG, originally discovered in Basset Hound)
  • Progressive Retinal Atrophy
    • CNGB1 variant (Papillon)
    • SAG variant (Basenji)
    • CNGA1 variant (Shetland Sheepdog)
    • GRPRA2 variant (Golden Retriever)
    • Autosomal Dominant
    • cone-rod dystrophy 1 (crd1)
    • cone-rod dystrophy 2 (crd2)
    • rod-cone dysplasia (rcd1)
    • rod-cone dysplasia (rcd1a)
    • rod-cone dysplasia (rcd3)
  • Congenital Hypothyroidism
  • Complement 3 (C3) deficiency
  • Cyclic Neutropaenia (CN, Gray Collie Syndrome)
  • Severe Combined Immunodeficiency (PRKDC variant)
  • Severe Combined Immunodeficiency (RAG1 variant)
  • X-linked Severe Combined Immunodeficiency
  • Cobalamin malabsorption
  • Fucosidosis
  • Gallbladder mucoceles
  • Glycogen Storage Disease Ia (Von Gierke Disease)
  • Glycogen Storage Disease II (Pompe's Disease)
  • Glycogen Storage Disease IIIa
  • Hypocatalasia
  • Imerslund-Grasbeck Syndrome (IGS, Cobalamin malabsorption)
  • Labrador obesity susceptibility
  • Lagotto Storage Disease
  • Lundehund syndrome
  • Menke's disease
  • Mucopolysaccharidosis I
  • Mucopolysaccharidosis IIIA
  • Mucopolysaccharidosis VI
  • Mucopolysaccharidosis VII
  • Periodic Fever Syndrome
  • Pyruvate dehydrogenase deficiency
  • Wilson's Disease (Copper toxicosis)
  • Inherited myopathy of Great Danes
  • Muscular Dystrophy
  • Muscular hypertrophy (Bully whippet syndrome)
  • Myotonia Congenita
  • Myotubular myopathy 1
  • Nemaline myopathy
  • Acral Mutilation Syndrome
  • Alaskan Husky Encephalopathy (Subacute nectrotising encephalopathy of Leigh)
  • Alexander disease
  • Axonal Disease Hypomyelination and Tremor
  • Benign Familiar Juvenile Epilepsy
  • Cerebellar Ataxia (RAB24 variant)
  • Cerebellar Ataxia (KCNJ10 variant)
  • Cerebellar Ataxia (ATP1B2 variant)
  • Cerebellar cortical degeneration
  • Deafness and vestibular dysfunction
  • Foetal-onset / neonatal neuroaxonal dystrophy
  • Generalised myoclonic epilepsy with photosensitivity
  • Juvenile euroaxonal dystrophy
  • L-2-hydroxyglutaricaciduria (L-2-HGA)
  • Leonberger Polyneuropathy
  • Narcolepsy
  • Neonatal Ataxia (NA, Bandera's Neonatal Ataxia, BNAt)
  • Neonatal Encephalopathy with seizures (NEWS)
  • Neuroaxonal dystrophy (PLA2G6 variant)
  • Neuroaxonal dystrophy (VPS11 variant)
  • Neuronal Ceroid Lipofuscinosis (NCL) variants 1, 10, 12, 2, 4A, 6, 7 and 8
  • Sensory Ataxic Neuropathy (SAN)
  • Shaking puppy syndrome (X-linked generalised tremor syndrome)
  • Spinocerebellar Ataxia (KCNJ10 variant - Late Onset Ataxia)
  • Congenital myasthenic syndrome (CMS, CHRNE variant)
  • Congenital myasthenic syndrome (CMS, COLQ variant)
  • Congenital myasthenic syndrome (CMS, CHAT variant)
  • Exercise-induced metabolic myopathy
  • Gangliosidosis GM1
  • Gangliosidosis GM2 (HEXA variant)
  • Gangliosidosis GM2 (HEXB variant)
  • Globoid Cell Leukodystrophy (Krabbe's Disease)
  • Greyhound Polyneuropathy
  • Leucodystrophy
  • Leukoencephalomyelopahty
  • Muscular Dystrophy (Limb-girdle type 2F)
  • Paroxysmal Dyskenesia
  • BTBD17-related embryonic lethality
  • Persistent Mullerian Duct Syndrome
  • Primary Ciliary Dyskinesia
  • Acute Respiratory Distress Syndrome (ARDS)
  • Brachycephaly
  • Chondrodysplasia
  • Craniomandibular osteopathy
  • Hereditary Vitamin D-resistant rickets
  • Musladin-Lueke syndrome (MLS)
  • Osteochondromatosis
  • Osteogeneisis Imperfecta (3 variants)
  • Skeletal dysplasia
  • Spondylocostal dysostosis
  • Albinism (OCA2 and SLC45A2 variants)
  • Anhidrotic Ectodermal Dysplasia
  • Dry Eye Curly Coat Syndrome
  • Dystrophic epidermolysis bullosa
  • Ectodermal dysplasia
  • Epidermolytic Hyperkeratosis
  • Focal non-epidermolytic palmoplantar keratoderma
  • Icthyosis
  • Lethal acrodermatitis
  • Ligneous membranitis
  • Palmoplantar hyperkeratosis (Hereditary footpad keratosis)
  • Recessive Hypotrichosis
  • Cystinuria Type I-A
  • Cystinuria Type II-A
  • Cystinuria Type II-B
  • Familial Nephropathy (FN)
  • Hyperuricosuria (HUU)
  • Primary Hyperoxaluria 
  • Renal Cystadenocarcinoma and Nodular Dermatofibrosis
  • X-linked nephropathy

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