^AKC DNA + Health Kit
^AKC DNA + Health Kit

^AKC DNA + Health Kit

​This kit requires activation using a sample key and activation code at https://dna.akc.org prior to submission. Failure to do so will result in delays in receiving results. Includes genetic identity for parentage verification and genetic health and traits testing. Does NOT determine dog breed.

$ 135.99

Additional Info

To purchase the AKC DNA Kit for just genetic identity and parentage verification without genetic health and trait markers click here.

AKC DNA + Health: A powerful breeder tool

Processing

  • Activate at dna.akc.org using the sample key and activation code assigned to each individual kit. 
  • Accurate results within  4-6 weeks.

Reporting: 

  • Results will be emailed to the customer’s address on file.
  • Report includes letter of analysis for the AKC DNA Profile, and report for health and traits results.

Please Note: AKC DNA testing DOES NOT determine breed of the dog (breed purity), conformation, performance ability, or specific coat color. AKC DNA health and trait tests are for informational purposes only. A normal result does not exclude a different cause of this disease, either from a different genetic variant, or from another cause. Abnormal results are not diagnostic for the disease. If you are concerned your dog may have this disease, please consult your veterinarian. Trait testing provides genotypes for color or trait markers, but does not determine specific color or traits.

The AKC DNA Health Test Kit is excluded from 30-day satisfaction guarantee

    Contact Us 

    Phone: 919-816-3508 

    Fax: 919-816-4255

    Email: dnahealth@akc.org 

    Benefits

    Included Tests

    •  AKC DNA Profile (201 markers for genetic identity)
    • 328 markers for health and traits

    Included Health Tests


    •    Common Disease Markers;
    o    Intervertebral Disc Disease Risk Factor & Chondrodystrophy (CDDY with IVDD)
    o    Collie Eye Anomaly (CEA, CH)
    o    Degenerative Myelopathy (DM) (Common Variant, SOD1A & Bernese Mountain Dog Variant, SOD1B)
    o    Exercise-Induced Collapse (EIC)
    o    Hyperuricosuria (HUU)
    o    Primary Lens Luxation (PLL)
    o    Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration (PRA-prcd, PRCD) and 24 other variants for PRA. Scroll down for more tests.

    •    Other Markers;
    o    Acral Mutilation Syndrome (AMS, SN)
    o    Acute Respiratory Distress Syndrome (ARDS)
    o    Adult Paroxysmal Dyskinesia (PxD, cPxD)
    o    Afibrinogenemia (Dachshund Type)
    o    Alaskan Husky Encephalopathy (AHE)
    o    Alaskan Malamute Polyneuropathy (AMPN)
    o    Amelogenesis Imperfecta (Italian Greyhound Type) (AI, ARAO)
    o    Amelogenesis Imperfecta (Parson Russell Terrier Type)
    o    Ataxia (Norwegian Buhund Type)
    o    Benign Familial Juvenile Epilepsy (BFJE)
    o    Bernard-Soulier Syndrome
    o    Canine Multiple System Degeneration (Chinese Crested Type) (CMSD)
    o    Canine Multiple System Degeneration (Kerry Blue Terrier Type) (CMSD, PNA)
    o    Canine Scott Syndrome (CSS)
    o    Cardiomyopathy and Juvenile Mortality
    o    Catalase Deficiency
    o    Centronuclear Myopathy (CNM)
    o    Cerebellar Ataxia (Finnish Hound Type)
    o    Cerebellar Ataxia 1 (Belgian Shepherd Type)
    o    Cerebellar Ataxia 2 (Belgian Shepherd Type)
    o    Cerebellar Cortical Degeneration
    o    Cerebellar Degeneration (HA, CA)
    o    Charcot-Marie-Tooth Disease
    o    Chondrodysplasia (Karelian Bear Dog & Norwegian Elkhound Type)
    o    Cleft Palate & Syndactyly (Nova Scotia Duck Tolling Retriever Type) (CP1, CLPS)
    o    Coagulation Factor VII Deficiency
    o    Complement 3 Deficiency
    o    Cone Degeneration (CD)
    o    Cone Degeneration (German Shepherd Dog Type) (CD)
    o    Cone Degeneration (German Shorthaired Pointer Type) (CD)
    o    Cone Degeneration (Labrador Retriever Type) (CD)
    o    Congenital Hypothyroidism with Goiter (Terrier Type) (CHG)
    o    Congenital Idiopathic Megaesophagus Risk Factor (German Shepherd Type)
    o    Congenital Macrothrombocytopenia (Cairn and Norfolk Terrier Type)
    o    Congenital Methemoglobinemia
    o    Congenital Myasthenic Syndrome (Golden Retriever Type)
    o    Congenital Myasthenic Syndrome (Jack Russell Terrier Type) (CMS)
    o    Congenital Myasthenic Syndrome (Labrador Retriever Type) (CMS)
    o    Congenital Myasthenic Syndrome (Old Danish Pointer Type) (CMS)
    o    Congenital Stationary Night Blindness (CSNB, LCA)
    o    Copper Storage Disease
    o    Craniomandibular Osteopathy (CMO)
    o    Cyclic Neutropenia (CH, CN)
    o    Cystinuria (Australian Cattle Dog Type)
    o    Cystinuria (Labrador Retriever Type)
    o    Cystinuria (Miniature Pinscher Type)
    o    Cystinuria (Newfoundland Type)
    o    Cystinuria Type 3 (Bulldog Risk Factor, Variants 1 & 2)
    o    Cystinuria Type 3 (Bulldog Risk Factor, Variant 3)
    o    Dandy-Walker-Like Malformation
    o    Darier Disease and Associated Infundibular Cyst Formation
    o    Deafness and Vestibular Dysfunction (Doberman Pinscher Type), Variant 2
    o    Dental Hypomineralization
    o    Diffuse Cystic Renal Dysplasia & Hepatic Fibrosis
    o    Dilated Cardiomyopathy (Doberman Pinscher Type Risk Factor, Variant 1) (DCM)
    o    Dilated Cardiomyopathy (Doberman Pinscher Type Risk Factor, Variant 2) (DCM)
    o    Dilated Cardiomyopathy (Schnauzer Type) (DCM)
    o    Dry Eye Curly Coat Syndrome (CKSID)
    o    Dystrophic Epidermolysis Bullosa (Basset Hound Type) (DEB)
    o    Dystrophic Epidermolysis Bullosa (Golden Retriever Type) (DEB)
    o    Early-Onset Adult Deafness (Rhodesian Ridgeback Type)
    o    Early Retinal Degeneration (ERD)
    o    Early  Onset Epilepsy (Parson Russell Terrier Type)
    o    Ectodermal Dysplasia (Chesapeake Bay Retriever Type) (ED)
    o    Ectodermal Dysplasia, X-Linked (Dachshund Type) (XLHED)
    o    Ectodermal Dysplasia, X-Linked (Shepherd Type) (XHED, XLED)
    o    Ehlers-Danlos Syndrome (Doberman Pinscher Type)
    o    Ehlers-Danlos Syndrome (Labrador Retriever Type), Variant 1
    o    Ehlers-Danlos Syndrome (Labrador Retriever Type), Variant 2
    o    Ehlers-Danlos Syndrome (Poodle Type, Variants 1 and 2) (EDS)
    o    Elliptocytosis
    o    Epidermolytic Hyperkeratosis
    o    Episodic Falling Syndrome (EDFS)
    o    Exfoliative Cutaneous Lupus Erythematosus (ECLE)
    o    Factor XI Deficiency 
    o    Familial Nephropathy (Cocker Spaniel Type) (FN, HN)
    o    Familial Nephropathy (English Springer Spaniel Type) (FN, HN)
    o    Fucosidosis
    o    Gallbladder Mucoceles
    o    Glanzmann’s Thrombasthenia (Great Pyrenees Type) (GT)
    o    Glanzmann’s Thrombasthenia (Otterhound Type) (GT)
    o    Glaucoma (Border Collie Type) (PCAD)
    o    Globoid Cell Leukodystrophy (Irish Setter Type) (GLD)
    o    Globoid Cell Leukodystrophy (Terrier Type) (GLD)
    o    Glycogen Storage Disease Ia (GSD Ia, GSD1a) 
    o    Glycogen Storage Disease IIIa (GSD IIIa)
    o    Glycogen Storage Disease VII (Wachtelhund Type) (GSD VII, PFK deficiency)
    o    Glycogen Storage Disease VII, PFK Deficiency (GSD VII, PFK deficiency)
    o    GM1 Gangliosidosis (Alaskan Husky Type)
    o    GM1 Gangliosidosis (Portuguese Water Dog Type)
    o    GM1 Gangliosidosis (Shiba Inu Type)
    o    GM2 Gangliosidosis (Japanese Chin Type)
    o    GM2 Gangliosidosis (Poodle Type)
    o    GM2 Gangliosidosis (Shiba Inu Type)
    o    Greyhound Polyneuropathy
    o    Hemophilia A (Boxer Type)
    o    Hemophilia A (German Shepherd Dog, Type 1)
    o    Hemophilia A (German Shepherd Dog, Type 2)
    o    Hemophilia A (Rhodesian Ridgeback Type)
    o    Hemophilia B (Cairn Terrier Type)
    o    Hemophilia B (Lhasa Apso Type)
    o    Hemophilia B (Rhodesian Ridgeback Type)
    o    Hereditary Ataxia (Australian Shepherd Type)
    o    Hereditary Cataracts (HC, JC)
    o    Hereditary Cataracts (Australian Shepherd Type) (HC, HSF4, JC)
    o    Hereditary Cataracts (Wirehaired Pointing Griffon Type)
    o    Hereditary Footpad Hyperkeratosis (Irish Terrier & Kromfohrländer Type)
    o    Hereditary Footpad Hyperkeratosis (Rottweiler Type)
    o    Hereditary Nasal Parakeratosis (Greyhound Type) (HNPK)
    o    Hereditary Nasal Parakeratosis (Labrador Retriever Type) (HNPK)
    o    Hereditary Nephritis (Samoyed Type) (AS, HN, XLHN)
    o    Hypomyelination (Weimaraner Type) (HYM, HS)
    o    Ichthyosis (American Bulldog Type)
    o    Ichthyosis (Golden Retriever Type 1)
    o    Ichthyosis (Golden Retriever Type 2)
    o    Ichthyosis (Great Dane Type)
    o    Ichthyosis (Jack Russell Terrier Type)
    o    Inflammatory Myopathy (Shepherd Type)
    o    Inherited Myopathy of Great Danes (IMGD)
    o    Intestinal Cobalamin Malabsorption (Beagle Type) (I-GS)
    o    Intestinal Cobalamin Malabsorption (Border Collie Type)
    o    Intestinal Cobalamin Malabsorption (Giant Schnauzer Type)
    o    Intestinal Lipid Malabsorption
    o    Junctional Epidermolysis Bullosa (Australian Shepherd Type)
    o    Juvenile Laryngeal Paralysis & Polyneuropathy (Black Russian Terrier Type) (JLPP, POANV)
    o    Juvenile Myoclonic Epilepsy (Rhodesian Ridgeback Type)
    o    L-2-Hydroxyglutaric Aciduria (Staffordshire Bull Terrier Type) (L-2-HGA) 
    o    L-2-Hydroxyglutaric Aciduria (Yorkshire Terrier Type) (L-2-HGA) 
    o    Lagotto Storage Disorder (LSD)
    o    Laryngeal Paralysis and Polyneuropathy (Leonberger Type 3)
    o    Late Onset Ataxia (LOA, SCA)
    o    Lethal Acrodermatitis (LAD)
    o    Leukocyte Adhesion Deficiency, Type I (CLAD, LAD-A)
    o    Leukocyte Adhesion Deficiency, Type III (CLAD, LAD-III)
    o    Ligneous Membranitis (LM)
    o    Limb-Girdle Muscular Dystrophy (Dachshund Type)
    o    Lundehund Syndrome (LS)
    o    Macular Corneal Dystrophy (Labrador Retriever Type) (MCD)
    o    Mammary Tumors (English Springer Spaniel Type Risk Factor)
    o    May-Hegglin Anomaly (MHA)
    o    Microphthalmia (Soft Coated Wheaten Terrier Type)
    o    Mucopolysaccharidosis I (Boston Terrier Type) (MPS I)
    o    Mucopolysaccharidosis I (Plott Hount Type) (MPS I)
    o    Mucopolysaccharidosis IIIA (Dachshund Type) (MPS IIIA)
    o    Mucopolysaccharidosis IIIA (New Zealand Huntaway Type) (MPS IIIA)
    o    Mucopolysaccharidosis IIIB (Schipperke Type) (MPS IIIB)
    o    Mucopolysaccharidosis VI (Miniature Schnauzer Type) (MPS VI)
    o    Mucopolysaccharidosis VII (Brazilian Terrier Type) (MPS VII)
    o    Mucopolysaccharidosis VII (Shepherd Type) (MPS VII)
    o    Multidrug Resistance 1 (MDR1)
    o    Multifocal Retinopathy 1 (CMR1)
    o    Multifocal Retinopathy 2 (CMR2)
    o    Multifocal Retinopathy 3 (CMR3)
    o    Muscular Dystrophy (Golden Retriever Type) (DMD, GRMD)
    o    Musladin-Lueke Syndrome (MLS)
    o    Myostatin Deficiency (Whippet)
    o    Myotonia Congenita (Australian Cattle Dog Type)
    o    Myotonia Congenita (Labrador Retriever Type)
    o    Myotonia Congenita (Schnauzer Type)
    o    Myotubular Myopathy 1 (Boykin Spaniel Type) (MTM1, XLMTM)
    o    Myotubular Myopathy 1 (Labrador Retriever Type) (MTM1, XLMTM)
    o    Myotubular Myopathy 1 (Rottweiler Type) (MTM1, XLMTM)
    o    Narcolepsy (Dachshund Type)
    o    Narcolepsy (Doberman Pinscher Type)
    o    Narcolepsy (Labrador Retriever Type)
    o    Neonatal Ataxia
    o    Neonatal Cerebellar Cortical Degeneration (NCCD)
    o    Neonatal Encephalopathy with Seizures (NEWS)
    o    Neuroaxonal Dystrophy (Giant Schnauzer Type) (NAD)
    o    Neuroaxonal Dystrophy (Papillon Type) (NAD)
    o    Neuroaxonal Dystrophy (Rottweiler Type) (NAD)
    o    Neuroaxonal Dystrophy (Spanish Water Dog Type) (NAD)
    o    Neuronal Ceroid Lipofuscinosis (Tibetan Terrier Type) (NCL)
    o    Neuronal Ceroid Lipofuscinosis 1 (NCL, NCL1)
    o    Neuronal Ceroid Lipofuscinosis 1 (Cane Corso Type) (NCL, NCL1)
    o    Neuronal Ceroid Lipofuscinosis 2 (NCL, NCL2)
    o    Neuronal Ceroid Lipofuscinosis 4A (NCL, NCL4A)
    o    Neuronal Ceroid Lipofuscinosis 5 (Golden Retriever Type) (NCL, NCL5)
    o    Neuronal Ceroid Lipofuscinosis 5 (Herding Dog Type) (NCL, NCL5)
    o    Neuronal Ceroid Lipofuscinosis 6 (NCL, NCL6)
    o    Neuronal Ceroid Lipofuscinosis 7 (NCL, NCL7)
    o    Neuronal Ceroid Lipofuscinosis 8 (Australian Shepherd Type) (NCL, NCL8)
    o    Neuronal Ceroid Lipofuscinosis 8 (Setter Type) (NCL, NCL8)
    o    Neuronal Ceroid Lipofuscinosis 10 (NCL, NCL10)
    o    Neuronal Ceroid Lipofuscinosis 12 (NCL, NCL12)
    o    Nonsyndromic Hearing Loss (Rottweiler Type)
    o    Oculocutaneous Albinism (Doberman Pinscher Type)(OCA)
    o    Oculocutaneous Albinism (Small Breed Type) (OCA)
    o    Osteochondrodysplasia
    o    Osteogenesis Imperfecta (Beagle Type) (OI)
    o    Osteogenesis Imperfecta (Dachshund Type) (OI)
    o    Osteogenesis Imperfecta (Golden Retriever Type) (OI)
    o    P2RY12 Receptor Platelet Disorder
    o    Pancreatitis (Miniature Schnauzer Type Risk Factor)
    o    Pembroke Welsh Corgi Duchenne Muscular Dystrophy (DMD)
    o    Persistent Müllerian Duct Syndrome (PMDS)
    o    Pituitary Dwarfism (Shepherd Type)
    o    Polyneuropathy (Leonberger & Saint Bernard Type) (PN)
    o    Polyneuropathy (Leonberger Type 2) (PN, LPN2)
    o    Polyneuropathy with Ocular Abnormalities & Neuronal Vacuolation (POANV, WMS1)
    o    Pompe Disease (GSD II)
    o    Prekallikrein Deficiency
    o    Primary Ciliary Dyskinesia (Alaskan Malamute Type) (PCD)
    o    Primary Ciliary Dyskinesia (Old English Sheepdog Type) (PCD)
    o    Primary Hyperoxaluria (PH1)
    o    Primary Lens Luxation (PLL)
    o    Primary Open Angle Glaucoma (POAG)
    o    Primary Open Angle Glaucoma (Basset Fauve de Bretagne Type) (POAG)
    o    Primary Open Angle Glaucoma (Basset Hound Type) (POAG)
    o    Primary Open Angle Glaucoma (Norwegian Elkhound Type) (POAG)
    o    Primary Open Angle Glaucoma & Primary Lens Luxation (Shar Pei Type) (POAG/PLL)
    o    Progressive Retinal Atrophy (Basenji Type) (PRA)
    o    Progressive Retinal Atrophy (Bullmastiff/Mastiff Type)
    o    Progressive Retinal Atrophy (Giant Schnauzer Type) (PRA, PRA5)
    o    Progressive Retinal Atrophy (Irish Setter Type) (PRA-rcd1)
    o    Progressive Retinal Atrophy (Shetland Sheepdog Type) (CNGA1-PRA, PRA)
    o    Progressive Retinal Atrophy (Sloughi Type Type) (PRA-rcd1a)
    o    Progressive Retinal Atrophy, Cone-Rod Dystrophy (Dachshund Type) (PRA-crd)
    o    Progressive Retinal Atrophy, Cone-Rod Dystrophy 1 (American Staffordshire Terrier Type) (PRA-crd1)
    o    Progressive Retinal Atrophy, Cone-Rod Dystrophy 2 (American Staffordshire Terrier Type) (PRA-crd2)
    o    Progressive Retinal Atrophy, Cone-Rod Dystrophy 3 (Glen of Imaal Terrier Type) (PRA-crd3)
    o    Progressive Retinal Atrophy, Cone-Rod Dystrophy 4 (PRA-crd4/cord1)
    o    Progressive Retinal Atrophy, Early Onset (Spanish Water Dog Type)
    o    Progressive Retinal Atrophy, Early-Onset (Portuguese Water Dog Type)
    o    Progressive Retinal Atrophy, Generalized (Schapendoes Type)
    o    Progressive Retinal Atrophy, Golden Retriever 1 (GR-PRA, GR1-PRA)
    o    Progressive Retinal Atrophy, Golden Retriever 2 (GR-PRA2, GR2-PRA)
    o    Progressive Retinal Atrophy, Late-Onset (Lapponian Herder Type)
    o    Progressive Retinal Atrophy, PRA1 (Papillon Type) (PRA, PRA1)
    o    Progressive Retinal Atrophy, PRA3 (Tibetan Terrier & Spaniel Type) (PRA3)
    o    Progressive Retinal Atrophy, Rod-Cone Dysplasia 3 (PRA-rcd3)
    o    Progressive Retinal Atrophy, Rod-Cone Dysplasia 4 (PRA-rcd4)
    o    Progressive Retinal Atrophy, Syndromic Retinal Degeneration (Shetland Sheepdog Type)
    o    Progressive Retinal Atrophy, X-Linked 1 (Husky Type) (XLPRA1)
    o    Progressive Retinal Atrophy, X-linked 2 (XLPRA2)
    o    Protein Losing Nephropathy
    o    Pyruvate Dehydrogenase Deficiency (PDP1)
    o    Pyruvate Kinase Deficiency (Basenji Type) (PKD)
    o    Pyruvate Kinase Deficiency (Beagle Type) (PKD)
    o    Pyruvate Kinase Deficiency (Labrador Retriever Type) (PKD)
    o    Pyruvate Kinase Deficiency (Pug Type Type) (PKD)
    o    Pyruvate Kinase Deficiency (Terrier Type) (PKD)
    o    Recurrent Inflammatory Pulmonary Disease (IPD)
    o    Renal Cystadenocarcinoma & Nodular Dermatofibrosis
    o    Retinal Dysplasia/Oculoskeletal Dysplasia 1 (OSD1, DRD1, RD/OSD1)
    o    Retinal Dysplasia/Oculoskeletal Dysplasia 2 (OSD2, DRD2, RD/OSD2)
    o    Sensory Neuropathy (Border Collie Type) (SN)
    o    Severe Combined Immunodeficiency Disease (Terrier Type) (SCID)
    o    Severe Combined Immunodeficiency Disease (Wetterhound Type) (SCID)
    o    Severe Combined Immunodeficiency Disease, X-Linked (Basset Hound Type) (XSCID)
    o    Severe Combined Immunodeficiency Disease, X-Linked (Corgi Type) (XSCID)
    o    Shar-Pei Autoinflammatory Disease (SPAID)
    o    Skeletal Dysplasia 2 (SD2)
    o    Spinal Dysraphism
    o    Spinocerebellar Ataxia (Alpine Dachsbrake Type) (SCA)
    o    Spinocerebellar Ataxia (Terrier Type) (SCA)
    o    Spondylocostal Dysostosis (SCD)
    o    Stargardt Disease (STGD)
    o    Startle Disease
    o    Subacute Necrotizing Encephalopathy (Yorkshire Terrier Type)
    o    Thrombopathia (American Eskimo Dog Type)
    o    Thrombopathia (Basset Hound Type)
    o    Thrombopathia (Newfoundland Type)
    o    Trapped Neutrophil Syndrome (TNS)
    o    Ullrich Congenital Muscular Dystrophy (Labrador Retriever Type 1)
    o    Ullrich Congenital Muscular Dystrophy (Labrador Retriever Type 2)
    o    Urolithiasis (Native American Indian Dog Type)
    o    Van Den Ende-Gupta Syndrome (VDEGS)
    o    Von Willebrand Disease I (VWDI)
    o    Von Willebrand Disease II (VWDII)
    o    Von Willebrand Disease III (Kooikerhondje Type) (VWDIII)
    o    Von Willebrand Disease III (Scottish Terrier Type) (VWDIII)
    o    Von Willebrand Disease III (Shetland Sheepdog Type) (VWDIII)

    Included Traits Tests 


    •    Coat Colors:
    o    A Locus (Agouti, Ay, Aw/at, a)
    o    As Locus (Saddle Tan)
    o    B Locus (Brown, ba, bc, bd, be, bh, bs)
    o    Co Locus (Cocoa, French Bulldog Type)
    o    D Locus (Dilute, d1, d2, & d3)
    o    E Locus (e1, e2, e3, eA, Eg, Eh, & Em)
    o    H Locus (Harlequin, Great Dane Type)
    o    I Locus (Intensity)
    o    K Locus (Dominant Black)
    o    M Locus (Merle)
    o    R Locus (Roan/Ticked)
    o    S Locus (White Spotting, Parti, or Piebald)
       
    •    Other Traits:
    o    Brachycephaly
    o    Chondrodysplasia (CDPA)
    o    Cu Locus (Curly)
    o    Hairlessness
    o    Hr Locus (FOXI3 Hairless Gene Test, Mexican Hairless, Peruvian Hairless and Chinese Crested Type)
    o    IC Locus (Improper Coat/Furnishings)
    o    L Locus (Long Hair/Fluffy)
    o    Polydactyly (Common Variant)
    o    Polydactyly (Great Pyrenees Type)
    o    Sex Determination
    o    SD Locus (Shedding)
    o    Social Behavior
    o    T Locus (Natural Bobtail)

    For a more detailed list of included tests, CLICK HERE
    For a list of breed-specific recommended tests, CLICK HERE

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