The Royal Kennel Club DNA Testing Services - Individual DNA tests

Explore our wide selection of individual DNA tests. Ideal for when a full breed-specific package isn't necessary, these tests let you select exactly what tests your dog requires.

Important Notice: We are currently experiencing significant delays with our DNA testing services due to a supplier issue. As a result, all test results will be delayed by a minimum of 5 weeks.

Please note that this timeframe is subject to change and may be extended.

Acral mutilation syndrome (AMS)

Alaskan Malamute polyneuropathy (AMPN)

Australian Shepherd Hereditary cataract (HC-HSF4)

Basset Hound Primary open angle glaucoma (POAG-3)

Canine leucocyte adhesion deficiency (CLAD)

Centronuclear myopathy (CNM)

Chondrodysplasia (CDSL)

Collie eye anomaly/Choroidal hypoplasia (CEA/CH)

Cone degeneration (CD)

Congenital Hypothyroidism with Goiter (CHG)

Congential stationary night blindness (CSNB)

Copper toxicosis (COMMD1)

Curly coat/dry eye (CC/DE)

Cystinuria (CU)

Degenerative myelopathy (DM)*

Dental hypomineralisation / Raine's Syndrome (Raine's synd)

Dilated cardiomyopathy (DCM)

Episodic falling (EF)*

Exercise induced collapse (EIC)*

Factor VII deficiency (FVIID)

Familial nephropathy (FN)

Fucosidosis (Fuco)

Glanzmann's Thrombastenia

Glycogen storage disease II (GSDII)

Greyhound neuropathy (GN)

Hereditary cataract (HC-HSF4-2)

Hereditary cerebellar ataxia (HCA)

Hereditary nasal parakeratosis (HNPK)*

Hyperuricosuria (HUU)

Ichthyosis (ICT-A)

Border Collie Imerslun-Gräsbeck syndrome/cobalamin malabsorption (IGS)

Beagle Imerslun-Gräsbeck syndrome/cobalamin malabsorption (IGS-2)

Inherited myopathy of Great Danes (IMGD)

Juvenile epilepsy (JE)

Juvenile laryngeal paralysis & Polyneuropathy (JLPP)

Juvenile myoclonic epilepsy (JME)

L2-hydroxyglutaric aciduria (L2-HGA)

Late onset ataxia (LOA)

Leonberger polyneuropathy (LNP1)

Leonberger polyneuropathy (LPN2)

Leukoencephalo- myelopathy (LEMP)

Leukoencephalo- myelopathy (LEMP-2)

Linkage test - Cerebellar ataxia (CA)

Lysosomal storage disease (LSD)

Macular corneal dystrophy (MCD)

Muco- polysaccharidosis type IIIB (MPSIIIB)

Multidrug resistance gene 1 (MDR1)

Musladin-Lueke syndrome (MLS)

Neonatal cerebellar cortical degeneration (NCCD)

Neuronal ceroid lipofuscinosis (NCL12)

Neuronal ceroid lipofuscinosis (NCL5)

Norwegian Elkhound Primary open angle glaucoma (POAG-2)

Osteochondro- dysplasia (OC)

Papillon Neuoraxonal dystrophy (NAD-PLA2G6)

PBGV Primary open angle glaucoma (POAG-5)

Phosphofructokinase deficiency (PFK)

Pituitary dwarfism (DP-LHX3)

Portuguese Water Dog Gangliosidosis (GM1)

Primary cillary dyskinesia (PCD)

Primary lens luxation (PLL)

Progressive retinal atrophy (BBS2-PRA)

Progressive retinal atrophy (CNGA1-PRA)

Progressive retinal atrophy (GR-PRA1)

Progressive retinal atrophy (GR-PRA2)

Progressive retinal atrophy (Pap-PRA 1)

Progressive retinal atrophy (PRA cord1)

Progressive retinal atrophy (PRA3)

Progressive retinal atrophy (PRA4)

Progressive retinal atrophy (PRA5)

Progressive retinal atrophy (PRA-crd3)

Progressive retinal atrophy (PRA-rcd1)

Progressive retinal atrophy (PRA-rcd3)

Progressive retinal atrophy (PRA-rcd4)

Progressive retinal atrophy (prcd-PRA)

Pyruvate dehydrogenase phosphates (PDP-1)

Retinopathy (PRA-MERTK)

Saluki Neuronal ceroid lipofuscinosis (SAL-NCL)

Sensory neuropathy (SN)

Severe goniodysgenesis & glaucoma risk (Gonio)

Shar Pei Primary open angle glaucoma/Primary lens luxation (POAG/PLL)

Skeletal dysplasia 2 (SD2)

Spanish Water Dog Neuroaxonal dystrophy (NAD-TECPR2)

Spinocerebellar ataxia (SCA)

Stargardt disease (STGD)

Trapped neutrophil syndrome (TNS)

von Willebrand disease type 1 (vWD I)

von Willebrand disease type 2 (vWD II)

von Willebrand disease type 3 (vWD III)

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