How to interpret these results:

AT RISK status: Testing positive (AT RISK) is predictive of your dog being affected by this condition, but it is not a final diagnosis nor does it predict when symptoms may occur or the severity of a condition in your dog.

CARRIER status: This indicates the dog has inherited a recessive allele for a genetic trait or mutation. This is not enough to cause symptoms of the disease, but is important to bear in mind if the dog ever has offspring.

Conditions:

 Not AT RISK for any conditions tested.

Breed Specific Genetic Conditions Tested:

190 variants not detected

Results

Factor VII Deficiency (F7 Exon 5)

Identified in Alaskan Malamutes

Variant not detected

Polyneuropathy, NDRG1 Malamute Variant (NDRG1 Exon 4)

Identified in Alaskan Malamutes

Variant not detected

Additional Genetic Health Conditions

The reports on this page are for genetic health conditions that have not been directly studied in research in the Alaskan Malamute breed:

Some of these conditions may be more relevant to your breeding program than others. For conditions where we detected a variant, we recommend exploring the results and speaking with your veterinarian to discuss if there is any known potential risk for your dog.   (None detected)

Results

Multiple Drug Sensitivity (MDR1)

Identified in Australian Cattle Dogs, Australian Shepherds, and more

Variant not detected

P2Y12 Receptor Platelet Disorder (P2Y12)

Identified in Greater Swiss Mountain Dogs

Variant not detected

Haemophilia B (F9 Exon 7, Terrier Variant)

Identified in Cairn Terriers

Variant not detected

Haemophilia B (F9 Exon 7, Rhodesian Ridgeback Variant)

Identified in Rhodesian Ridgebacks

Variant not detected

Haemophilia A (F8 Exon 10, Boxer Variant)

Identified in Boxers

Variant not detected

Haemophilia A (F8 Exon 11, Shepherd Variant 1)

Identified in Berger Blanc Suisse, Czechoslovakian Vlcaks, and more

Variant not detected

Haemophilia A (F8 Exon 1, Shepherd Variant 2)

Identified in Berger Blanc Suisse, Czechoslovakian Vlcaks, and more

Variant not detected

Thrombopathia (RASGRP1 Exon 5, Basset Hound Variant)

Identified in Basset Hounds

Variant not detected

Thrombopathia (RASGRP1 Exon 8)

Identified in Landseers and Newfoundlands

Variant not detected

Thrombopathia (RASGRP1 Exon 5, American Eskimo Dog Variant)

Identified in American Eskimo Dogs

Variant not detected

Von Willebrand Disease Type III, Type III vWD (VWF Exon 4)

Identified in Cesky Terriers and Scottish Terriers

Variant not detected

Von Willebrand Disease Type III, Type III vWD (VWF Exon 7)

Identified in Shetland Sheepdogs

Variant not detected

Von Willebrand Disease Type I (VWF)

Identified in Australian Terriers, Barbets, and more

Variant not detected

Von Willebrand Disease Type II, Type II vWD (VWF)

Identified in German Longhaired Pointers, German Shorthaired Pointers, and more

Variant not detected

Canine Leukocyte Adhesion Deficiency Type I, CLADI (ITGB2)

Identified in Irish Red and White Setters and Irish Setters

Variant not detected

Canine Leukocyte Adhesion Deficiency Type III, CLADIII (FERMT3)

Identified in Berger Blanc Suisse, Czechoslovakian Vlcaks, and more

Variant not detected

Congenital Macrothrombocytopenia (TUBB1 Exon 1, Cairn and Norfolk Terrier Variant)

Identified in Cairn Terriers, Norfolk Terriers, and more

Variant not detected

Canine Elliptocytosis (SPTB Exon 30)

Identified in English Labrador Retrievers and Labrador Retrievers

Variant not detected

Glanzmann's Thrombasthenia Type I (ITGA2B Exon 12)

Identified in Otterhounds

Variant not detected

May-Hegglin Anomaly (MYH9)

Identified in Pugs

Variant not detected

Prekallikrein Deficiency (KLKB1 Exon 8)

Identified in Shih Tzus

Variant not detected

Pyruvate Kinase Deficiency (PKLR Exon 5)

Identified in Basenjis

Variant not detected

Pyruvate Kinase Deficiency (PKLR Exon 7 Labrador Variant)

Identified in English Labrador Retrievers and Labrador Retrievers

Variant not detected

Pyruvate Kinase Deficiency (PKLR Exon 7 Pug Variant)

Identified in Pugs

Variant not detected

Pyruvate Kinase Deficiency (PKLR Exon 7 Beagle Variant)

Identified in Beagles

Variant not detected

Pyruvate Kinase Deficiency (PKLR Exon 10)

Identified in Cairn Terriers and West Highland White Terriers

Variant not detected

Trapped Neutrophil Syndrome (VPS13B)

Identified in Border Collies, English Shepherds, and more

Variant not detected

Ligneous Membranitis, LM (PLG)

Identified in Scottish Terriers

Variant not detected

Platelet factor X receptor deficiency, Scott Syndrome (TMEM16F)

Identified in Berger Blanc Suisse, Czechoslovakian Vlcaks, and more

Variant not detected

Methemoglobinemia CYB5R3

Identified in Pomeranians

Variant not detected

Congenital Hypothyroidism (TPO, Tenterfield Terrier Variant)

Identified in Tenterfield Terriers

Variant not detected

Congenital Hypothyroidism (TPO, Rat, Toy, Hairless Terrier Variant)

Identified in American Hairless Terriers, Wire Fox Terriers, and more

Variant not detected

Complement 3 Deficiency, C3 Deficiency (C3)

Identified in Brittanys

Variant not detected

Severe Combined Immunodeficiency (PRKDC)

Identified in Jack Russell Terriers, Parson Russell Terriers, and more

Variant not detected

Severe Combined Immunodeficiency (RAG1)

Identified in Wetterhouns

Variant not detected

X-linked Severe Combined Immunodeficiency (IL2RG Variant 1)

Identified in Basset Hounds

Variant not detected

X-linked Severe Combined Immunodeficiency (IL2RG Variant 2)

Identified in Cardigan Welsh Corgis and Pembroke Welsh Corgis

Variant not detected

Progressive Retinal Atrophy, rcd1 (PDE6B Exon 21 Irish Setter Variant)

Identified in Irish Red and White Setters and Irish Setters

Variant not detected

Progressive Retinal Atrophy, rcd3 (PDE6A)

Identified in Cardigan Welsh Corgis, Chinese Cresteds, and more

Variant not detected

Progressive Retinal Atrophy, CNGA (CNGA1 Exon 9)

Identified in Shetland Sheepdogs

Variant not detected

Progressive Retinal Atrophy, prcd (PRCD Exon 1)

Identified in American Eskimo Dogs, American Hairless Terriers, and more

Variant not detected

Progressive Retinal Atrophy (CNGB1)

Identified in Papillons

Variant not detected

Progressive Retinal Atrophy (SAG)

Identified in Basenjis

Variant not detected

Golden Retriever Progressive Retinal Atrophy 1, GR-PRA1 (SLC4A3)

Identified in Golden Retrievers and Lhasa Apsos

Variant not detected

Golden Retriever Progressive Retinal Atrophy 2, GR-PRA2 (TTC8)

Identified in English Labrador Retrievers, Golden Retrievers, and more

Variant not detected

Progressive Retinal Atrophy, crd1 (PDE6B)

Identified in American Bullies, American Pit Bull Terriers, and more

Variant not detected

Progressive Retinal Atrophy - crd4/cord1 (RPGRIP1)

Identified in Beagles, Boykin Spaniels, and more

Variant not detected

X-Linked Progressive Retinal Atrophy 1, XL-PRA1 (RPGR)

Identified in Samoyeds, Siberian Huskies, and more

Variant not detected

Progressive Retinal Atrophy, PRA3 (FAM161A)

Identified in Tibetan Spaniels and Tibetan Terriers

Variant not detected

Collie Eye Anomaly (NHEJ1)

Identified in Australian Cattle Dogs, Australian Shepherds, and more

Variant not detected

Cone Degeneration (CNGB3 Exon 6)

Identified in German Shorthaired Pointers and Pointers

Variant not detected

Day Blindness (CNGA3 Exon 7 German Shepherd Variant)

Identified in Berger Blanc Suisse, Czechoslovakian Vlcaks, and more

Variant not detected

Day Blindness (CNGA3 Exon 7 Labrador Retriever Variant)

Identified in English Labrador Retrievers and Labrador Retrievers

Variant not detected

Autosomal Dominant Progressive Retinal Atrophy (RHO)

Identified in Bullmastiffs and Mastiffs

Variant not detected

Canine Multifocal Retinopathy (BEST1 Exon 2)

Identified in American Bullies, Australian Shepherds, and more

Variant not detected

Canine Multifocal Retinopathy (BEST1 Exon 5)

Identified in Coton de Tulears

Variant not detected

Canine Multifocal Retinopathy (BEST1 Exon 10 Deletion)

Identified in Finnish Lapphunds, Lapponian Herders, and more

Variant not detected

Canine Multifocal Retinopathy (BEST1 Exon 10 SNP)

Identified in Lapponian Herders and Swedish Lapphunds

Variant not detected

Glaucoma (ADAMTS10 Exon 9)

Identified in Norwegian Elkhounds

Variant not detected

Glaucoma (ADAMTS10 Exon 17)

Identified in Beagles

Variant not detected

Glaucoma (ADAMTS17 Exon 11)

Identified in Basset Fauve de Bretagnes

Variant not detected

Glaucoma (ADAMTS17 Exon 2)

Identified in Chinese Shar-Peis

Variant not detected

Goniodysgenesis and Glaucoma (OLFM3)

Identified in Border Collies

Variant not detected

Hereditary Cataracts (HSF4 Exon 9 Shepherd Variant)

Identified in Australian Shepherds, Australian Shepherds, and more

Variant not detected

Primary Lens Luxation (ADAMTS17)

Identified in American Eskimo Dogs, American Hairless Terriers, and more

Variant not detected

Congenital Stationary Night Blindness (RPE65)

Identified in Briards

Variant not detected

Macular Corneal Dystrophy, MCD (CHST6)

Identified in English Labrador Retrievers and Labrador Retrievers

Variant not detected

2-DHA Kidney & Bladder Stones (APRT)

Identified in American Indian Dogs

Variant not detected

Cystinuria Type I-A (SLC3A1)

Identified in Landseers and Newfoundlands

Variant not detected

Cystinuria Type II-A (SLC3A1)

Identified in Australian Cattle Dogs, Australian Kelpies, and more

Variant not detected

Cystinuria Type II-B (SLC7A9)

Identified in Miniature Pinschers

Variant not detected

Urate Kidney & Bladder Stones (SLC2A9)

Identified in American Bullies, American Pit Bull Terriers, and more

Variant not detected

Polycystic Kidney Disease, PKD (PKD1)

Identified in Bull Terriers

Variant not detected

Oxalate Kidney & Bladder Stones (AGXT)

Identified in Coton de Tulears

Variant not detected

Protein Losing Nephropathy, PLN (NPHS1)

Identified in Airedale Terriers and Soft Coated Wheaten Terriers

Variant not detected

X-Linked Hereditary Nephropathy, XLHN (COL4A5 Exon 35, Samoyed Variant 2)

Identified in Samoyeds and Samoyeds

Variant not detected

Autosomal Recessive Hereditary Nephropathy, Familial Nephropathy, ARHN (COL4A4 Exon 3)

Identified in Cocker Spaniels, English Cocker Spaniels, and more

Variant not detected

Primary Ciliary Dyskinesia, PCD (CCDC39 Exon 3)

Identified in Old English Sheepdogs

Variant not detected

Dry Eye Curly Coat Syndrome (FAM83H Exon 5)

Identified in Cavalier King Charles Spaniels and English Toy Spaniels

Variant not detected

Anhidrotic Ectodermal Dysplasia (EDA Intron 8)

Identified in Berger Blanc Suisse, Czechoslovakian Vlcaks, and more

Variant not detected

Renal Cystadenocarcinoma and Nodular Dermatofibrosis (FLCN Exon 7)

Identified in Berger Blanc Suisse, Czechoslovakian Vlcaks, and more

Variant not detected

Canine Fucosidosis (FUCA1)

Identified in English Springer Spaniels

Variant not detected

Pompe's Disease (GAA)

Identified in Finnish Lapphunds, Lapponian Herders, and more

Variant not detected

Glycogen Storage Disease Type IA, Von Gierke Disease, GSD IA (G6PC)

Identified in Malteses

Variant not detected

Glycogen Storage Disease Type IIIA, GSD IIIA (AGL)

Identified in Curly-Coated Retrievers

Variant not detected

Mucopolysaccharidosis Type I, MPS I (IDUA)

Identified in Plotts

Variant not detected

Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A, MPS IIIA (SGSH Exon 6 Variant 1)

Identified in Dachshunds, Dachshunds, and more

Variant not detected

Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A, MPS IIIA (SGSH Exon 6 Variant 2)

Identified in New Zealand Huntaways

Variant not detected

Mucopolysaccharidosis Type VII, Sly Syndrome, MPS VII (GUSB Exon 5)

Identified in Terrier Brasileiros

Variant not detected

Mucopolysaccharidosis Type VII, Sly Syndrome, MPS VII (GUSB Exon 3)

Identified in Belgian Laekenois, Belgian Malinois, and more

Variant not detected

Glycogen storage disease Type VII, Phosphofructokinase Deficiency, PFK Deficiency (PFKM Whippet and English Springer Spaniel Variant)

Identified in Boykin Spaniels, Cocker Spaniels, and more

Variant not detected

Glycogen storage disease Type VII, Phosphofructokinase Deficiency, PFK Deficiency (PFKM Wachtelhund Variant)

Identified in Deutscher Wachtelhunds

Variant not detected

Lagotto Storage Disease (ATG4D)

Identified in Lagotto Romagnolos

Variant not detected

Neuronal Ceroid Lipofuscinosis 1, NCL 1 (PPT1 Exon 8)

Identified in Dachshunds, Dachshunds, and more

Variant not detected

Neuronal Ceroid Lipofuscinosis 2, NCL 2 (TPP1 Exon 4)

Identified in Dachshunds and more

Variant not detected

Neuronal Ceroid Lipofuscinosis 1, Cerebellar Ataxia, NCL4A (ARSG Exon 2)

Identified in American Bullies, American Pit Bull Terriers, and more

Variant not detected

Neuronal Ceroid Lipofuscinosis 1, NCL 5 (CLN5 Border Collie Variant)

Identified in Australian Cattle Dogs, Border Collies, and more

Variant not detected

Neuronal Ceroid Lipofuscinosis 6, NCL 6 (CLN6 Exon 7)

Identified in Australian Shepherds, Australian Shepherds, and more

Variant not detected

Neuronal Ceroid Lipofuscinosis 8, NCL 8 (CLN8 English Setter Variant)

Identified in English Setters, Gordon Setters, and more

Variant not detected

Neuronal Ceroid Lipofuscinosis (MFSD8)

Identified in Chihuahuas and Chinese Cresteds

Variant not detected

Neuronal Ceroid Lipofuscinosis (CLN8 Australian Shepherd Variant)

Identified in Australian Cattle Dogs, Australian Shepherds, and more

Variant not detected

Neuronal Ceroid Lipofuscinosis 10, NCL 10 (CTSD Exon 5)

Identified in American Bullies, Alapaha Blue Blood Bulldogs, and more

Variant not detected

Neuronal Ceroid Lipofuscinosis (CLN5 Golden Retriever Variant)

Identified in Golden Retrievers

Variant not detected

Adult-Onset Neuronal Ceroid Lipofuscinosis (ATP13A2, Tibetan Terrier Variant)

Identified in Tibetan Terriers

Variant not detected

Late-Onset Neuronal Ceroid Lipofuscinosis (ATP13A2, Australian Cattle Dog Variant)

Identified in Australian Cattle Dogs, Australian Kelpies, and more

Variant not detected

GM1 Gangliosidosis (GLB1 Exon 15 Shiba Inu Variant)

Identified in Shiba Inus

Variant not detected

GM1 Gangliosidosis (GLB1 Exon 15 Alaskan Husky Variant)

Identified in Siberian Huskies

Variant not detected

GM1 Gangliosidosis (GLB1 Exon 2)

Identified in Portuguese Water Dogs

Variant not detected

GM2 Gangliosidosis (HEXB, Poodle Variant)

Identified in Standard Poodles, Miniature Poodles, and more

Variant not detected

GM2 Gangliosidosis (HEXA)

Identified in Japanese Chins

Variant not detected

Globoid Cell Leukodystrophy, Krabbe disease (GALC Exon 5)

Identified in Cairn Terriers and West Highland White Terriers

Variant not detected

Enamel Hypoplasia (Italian Greyhound Variant)

Identified in Italian Greyhounds

Variant not detected

Enamel Hypoplasia (Parson Russell Terrier Variant)

Identified in Parson Russell Terriers and Russell-type Terriers

Variant not detected

Persistent Mullerian Duct Syndrome, PMDS (AMHR2)

Identified in Miniature Schnauzers and Standard Schnauzers

Variant not detected

Deafness and Vestibular Syndrome of Dobermans, DVDob, DINGS (MYO7A)

Identified in Doberman Pinschers

Variant not detected

Shar-Pei Autoinflammatory Disease, SPAID, Shar-Pei Fever (MTBP)

Identified in Chinese Shar-Peis

Variant not detected

Alaskan Husky Encephalopathy (SLC19A3)

Variant not detected

Alexander Disease (GFAP)

Identified in English Labrador Retrievers and Labrador Retrievers

Variant not detected

Neonatal Cerebellar Cortical Degeneration (SPTBN2)

Identified in Beagles

Variant not detected

Early Onset Cerebellar Ataxia (SEL1L)

Identified in Finnish Hounds and Norrbottenspitzes

Variant not detected

Cerebellar Hypoplasia (VLDLR)

Identified in Eurasiers

Variant not detected

Late Onset Spinocerebellar Ataxia (CAPN1)

Identified in Jack Russell Terriers, Parson Russell Terriers, and more

Variant not detected

Spinocerebellar Ataxia with Myokymia and/or Seizures (KCNJ10)

Identified in Basenjis, Chihuahuas, and more

Variant not detected

Hereditary Ataxia (RAB24)

Identified in Gordon Setters and Old English Sheepdogs

Variant not detected

Juvenile Epilepsy (LGI2)

Identified in Lagotto Romagnolos

Variant not detected

Degenerative Myelopathy, DM (SOD1A)

Identified in American Eskimo Dogs, Berger Blanc Suisse, and more

Variant not detected

Fetal-Onset Neonatal Neuroaxonal Dystrophy (MFN2)

Identified in Giant Schnauzers

Variant not detected

Hypomyelination and Tremors (FNIP2)

Identified in Weimaraners

Variant not detected

Shaking Puppy Syndrome (PLP)

Identified in English Springer Spaniels

Variant not detected

Neuroaxonal Dystrophy, NAD (Spanish Water Dog Variant)

Identified in Spanish Water Dogs

Variant not detected

Neuroaxonal Dystrophy, NAD (Rottweiler Variant)

Identified in Rottweilers

Variant not detected

L-2-Hydroxyglutaricaciduria, L2HGA (L2HGDH)

Identified in American Bullies, American Pit Bull Terriers, and more

Variant not detected

Neonatal Encephalopathy with Seizures, NEWS (ATF2)

Identified in Standard Poodles, Miniature Poodles, and more

Variant not detected

Polyneuropathy, NDRG1 Greyhound Variant (NDRG1 Exon 15)

Identified in Greyhounds

Variant not detected

Narcolepsy (HCRTR2 Intron 6)

Identified in English Labrador Retrievers and Labrador Retrievers

Variant not detected

Canine Multiple System Degeneration (SERAC1 Exon 15)

Identified in Kerry Blue Terriers

Variant not detected

Canine Multiple System Degeneration (SERAC1 Exon 4)

Identified in Chinese Cresteds

Variant not detected

Juvenile Laryngeal Paralysis and Polyneuropathy (RAB3GAP1, Rottweiler Variant)

Identified in Black Russian Terriers and Rottweilers

Variant not detected

Acral Mutilation Syndrome (GDNF-AS)

Identified in Cocker Spaniels, English Cocker Spaniels, and more

Variant not detected

Leonberger Polyneuropathy 1 (LPN1, ARHGEF10)

Identified in Leonbergers and Saint Bernards

Variant not detected

Juvenile Myoclonic Epilepsy (DIRAS1)

Identified in Rhodesian Ridgebacks

Variant not detected

Leonberger Polyneuropathy 2 (GJA9)

Identified in Leonbergers

Variant not detected

Spongy Degeneration with Cerebellar Ataxia 1 (KCNJ10)

Identified in Belgian Laekenois, Belgian Malinois, and more

Variant not detected

Spongy Degeneration with Cerebellar Ataxia 2 (ATP1B2)

Identified in Belgian Laekenois, Belgian Malinois, and more

Variant not detected

Dilated Cardiomyopathy, DCM1 (PDK4)

Identified in Doberman Pinschers

Variant not detected

Dilated Cardiomyopathy, DCM2 (TTN)

Identified in Doberman Pinschers

Variant not detected

Long QT Syndrome (KCNQ1)

Identified in English Springer Spaniels

Variant not detected

Muscular Dystrophy (DMD, Cavalier King Charles Spaniel Variant 1)

Identified in Cavalier King Charles Spaniels and English Toy Spaniels

Variant not detected

Muscular Dystrophy (DMD Pembroke Welsh Corgi Variant )

Identified in Pembroke Welsh Corgis

Variant not detected

Muscular Dystrophy (DMD Golden Retriever Variant)

Identified in Golden Retrievers

Variant not detected

Limb Girdle Muscular Dystrophy (SGCD, Boston Terrier Variant)

Identified in Boston Terriers

Variant not detected

Centronuclear Myopathy (PTPLA)

Identified in English Labrador Retrievers and Labrador Retrievers

Variant not detected

Exercise-Induced Collapse (DNM1)

Identified in Bouvier des Flandress, Boykin Spaniels, and more

Variant not detected

Inherited Myopathy of Great Danes (BIN1)

Identified in Great Danes

Variant not detected

Bully Whippet Syndrome (MSTN)

Identified in Whippets

Variant not detected

Myotonia Congenita (CLCN1 Exon 7)

Identified in Miniature Schnauzers and Standard Schnauzers

Variant not detected

Myotonia Congenita (CLCN1 Exon 23)

Identified in Australian Cattle Dogs, Border Collies, and more

Variant not detected

X-Linked Myotubular Myopathy (MTM1, Labrador Variant)

Identified in English Labrador Retrievers and Labrador Retrievers

Variant not detected

Hypocatalasia, Acatalasemia (CAT)

Identified in Beagles

Variant not detected

Pyruvate Dehydrogenase Deficiency (PDP1)

Identified in Clumber Spaniels and Sussex Spaniels

Variant not detected

Malignant Hyperthermia (RYR1)

Identified in Greyhounds and Hungarian Greyhounds

Variant not detected

Cobalamin Malabsorption (CUBN Exon 53)

Identified in Border Collies and Australian Kelpies

Variant not detected

Cobalamin Malabsorption (CUBN Exon 8)

Identified in Beagles

Variant not detected

Lundehund Syndrome (LEPREL1)

Identified in Norwegian Lundehunds

Variant not detected

Congenital Myasthenic Syndrome (CHAT)

Identified in Old Danish Pointing Dogs

Variant not detected

Congenital Myasthenic Syndrome (COLQ)

Identified in English Labrador Retrievers and Labrador Retrievers

Variant not detected

Episodic Falling Syndrome (BCAN)

Identified in Cavalier King Charles Spaniels and English Toy Spaniels

Variant not detected

Paroxysmal Dyskinesia, PxD (PGIN)

Identified in Soft Coated Wheaten Terriers

Variant not detected

Dystrophic Epidermolysis Bullosa (COL7A1)

Identified in Golden Retrievers

Variant not detected

Skin Fragility Syndrome (PKP1)

Identified in Chesapeake Bay Retrievers

Variant not detected

Ichthyosis, Epidermolytic Hyperkeratosis (KRT10)

Identified in Norfolk Terriers and Lucas Terriers

Variant not detected

Ichthyosis (PNPLA1)

Identified in Golden Retrievers

Variant not detected

Ichthyosis (SLC27A4)

Identified in Great Danes

Variant not detected

Ichthyosis (NIPAL4)

Identified in American Bullies, Alapaha Blue Blood Bulldogs, and more

Variant not detected

Pachyonychia Congenita (KRT16)

Identified in Dogue de Bordeauxs

Variant not detected

Hereditary Footpad Hyperkeratosis (FAM83G)

Identified in Bedlington Terriers, Irish Terriers, and more

Variant not detected

Hereditary Nasal Parakeratosis (SUV39H2)

Identified in English Labrador Retrievers and Labrador Retrievers

Variant not detected

Musladin-Lueke Syndrome (ADAMTSL2)

Identified in Beagles

Variant not detected

Oculocutaneous Albinism, OCA2 (Pekingese Type)

Identified in Lhasa Apsos, Pekingese, and more

Variant not detected

Bald Thigh Syndrome (IGFBP5)

Identified in Greyhounds, Italian Greyhounds, and more

Variant not detected

Cleft Lip and/or Cleft Palate (ADAMTS20)

Identified in Nova Scotia Duck Tolling Retrievers

Variant not detected

Hereditary Vitamin D-Resistant Rickets (VDR)

Identified in Pomeranians

Variant not detected

Osteogenesis Imperfecta (COL1A2)

Identified in Beagles

Variant not detected

Osteogenesis Imperfecta (SERPINH1)

Identified in Dachshunds, Dachshunds, and more

Variant not detected

Osteogenesis Imperfecta (COL1A1)

Identified in Golden Retrievers

Variant not detected

Osteochondrodysplasia (SLC13A1)

Identified in Standard Poodles, Miniature Poodles, and more

Variant not detected

Skeletal Dysplasia 2, SD2 (COL11A2)

Identified in English Labrador Retrievers and Labrador Retrievers

Variant not detected

Craniomandibular Osteopathy, CMO (SLC37A2)

Identified in Australian Shepherds, Australian Shepherds, and more

Variant not detected

Intervertebral Disc Disease (Type I) (FGF4 retrogene - CFA12)

Identified in Basset Hounds, Beagles, and more

Variant not detected

Chondrodystrophy (ITGA10)

Identified in Norwegian Elkhounds, Karelian Bear Dogs, and more

Variant not detected