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Includes the following:

• A Locus (Fawn/Sable;Tri/Tan Points)
• Autosomal Hereditary Recessive Nephropathy
• Brown Coat Colour Profile
• Canine DNA Profile (Unique Identifier for Parentage)
• Canine Hyperuricosuria
• Centronuclear Myopathy (Labrador Retriever Type)
• Cone-Rod Dystrophy I - PRA (cord I)
• Congenital Myasthenic Syndrome (Labrador Retriever Type)
• Copper Toxicosis (ATP7B & ATP7A) Labrador Retriever Type
• Cystinuria (SLC3A1) Labrador Retriever Type
• D (Dilute) Locus
• Degenerative Myelopathy
• E Locus - (Cream/Red/Yellow)
• EM (MC1R) Locus - Melanistic Mask
• Elliptocytosis B-spectrin (Labrador Retriever/Poodle Type)
• Exercise Induced Collapse (Retriever Type)
• Gangliosidosis GM2 (Poodle Type)
• Generalised PRA 1 (Golden Retriever Type)
• Globoid Cell Leukodystrophy/Krabbe’s Disease
• Hereditary Nasal Parakeratosis/Dry Nose (Labrador Retriever Type)
• Ivermectin Sensitivity MDR1 (Multi Drug Resistance)
• K Locus (Dominant Black)
• Long Hair Gene (Canine)
• Malignant Hyperthermia
• Mild Disproportionate Dwarfism (Labrador Type)
• Mucopolysaccharidosis VI (Poodle Type)
• Myotubular Myopathy X-Linked (Labrador Retriever Type)
• Narcolepsy (Labrador)
• Neonatal Encephalopathy (Poodle Type)
• Phosphofructokinase Deficiency (Spaniel Type)
• Progressive Rod Cone Degeneration (prcd) - PRA
• Pyruvate Kinase Deficiency (Canine)
• Skeletal Dysplasia 2 (Dwarfism SD2)
• Skull Diversity (All Breeds)
• Weight and Appetite Obesity Prone (Labrador Retriever Type)
• Wire Hair Gene
• von Willebrand's Disease Type I