Acral mutilation syndrome
Amelogenesis imperfecta, ENAM-related
Ancient Red (eA)
Ataxia, cerebellar, KCNJ10-related
Brachycephaly
Brown color (bc)
Canine Multifocal Retinopathy (CMR1)
Canine Multifocal Retinopathy (CMR2)
Canine Scott Syndrome
Chondrodystrophy
Coat colour, agouti (recessive black)
Coat colour, grizzle
Coat colour, melanistic mask
Color Dilution (d1)
Color Dilution (d2)
Cystinuria Type I-A
Deafness, LOXHD1-related
Degenerative Myelopathy
Dew Claws
Epidermolysis bullosa, simplex, PLEC-related
Epilepsy, benign familial juvenile, LGI2-related
Exercise induced metabolic myopathy
Exercise-Induced Collapse
Fecundity, GDF9-related
Hair, long
Height, IGF1-AS-associated body-size variation
Hereditary Ataxia
Hereditary Footpad Hyperkeratosis
Hyperkeratosis, epidermolytic
Hypocatalasia
Hyposegmentation of granulocytes
Laryngeal paralysis and polyneuropathy, CNTNAP1 related
Lens luxation
Lethal Acrodermatitis
Leukocyte adhesion deficiency, type I
Leukoencephalomyelopathy
Lundehund syndrome
Metabolizer of a cognitive enhancer
Methaemoglobinaemia, CYB5R3-related
Nasal parakeratosis
Neuronal ceroid lipofuscinosis, 8
Persistent Mullerian Duct Syndrome (PMDS)
Prekallikrein deficiency
Primary Open Angle Glaucoma
Progressive retinal atrophy, NECAP1-related
Progressive rod-cone degeneration
Protein Losing Nephropathy
Red Pigment Intensity (I/i)
Shedding (T)
Skeletal Dysplasia 3
Spinocerebellar ataxia
Spongy degeneration with cerebellar ataxia 1
Tail, short
Thrombocytopenia, TUBB1-related
Upper Airway Syndrome
Urolithiasis
Von Willebrand Disease Type I
Von Willebrand Disease Type II
The test identifies potential risks for certain conditions and traits, but having these risks doesn't mean they will definitely develop.
