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Doberman Pinscher

Doberman Pinscher
Photo: Miroslav Cacik / Copyrighted free use · Wikimedia

117 Doberman Pinschers in the atlas. Every number on this page has a source.

Population-genetic snapshot of Doberman Pinschers in the Sniff Atlas, source-graded Mendelian carrier frequencies from Donner 2023, and nutrition guidance tied to the genetic findings above.

Also known as Doberman, Doberman Pincher, Doberman, Standard Pinscher, and Dobermann.

The plain version

Doberman Pinschers come from a somewhat limited gene pool, meaning their genetics are fairly similar across the breed. They typically weigh around 84 pounds and usually live about 11 years. Their look is sleek and strong, and they share some traits with breeds like the Giant Schnauzer and Great Pyrenees. Right now, no specific genetic health concerns have been identified in this breed’s overall gene pool, but it’s always a good idea to talk with your vet about any health testing.

What the atlas says about Doberman Pinscher

In the atlas, the Doberman Pinscher clusters consistently as Doberman Pinscher (100% of the 117 dogs here). At the trait loci, LCORL runs lower than average (6% here vs 83%); STC2 runs lower than average (5% here vs 74%).

Ranks 10 of 107 on the bottleneck severity scale, among the most genetically contracted breeds in the atlas.

Genetic dimensions · CanVAS atlas

What the genome says about Doberman Pinscher

Computed from the 18,477 research dogs in the Atlas.

Dogs in the Atlas
117Founders
39 from Momozawa, 25 from Hayward2016, 23 from Shannon
Genetic diversity
0.24Tight
Mean heterozygosity across the breed. Ranks 10th most genetically tight of 107 ranked breeds.
What does genetic diversity mean?

How varied a breed's gene pool is — the share of gene spots where a typical dog of the breed carries two different versions rather than two identical ones.

How to read it: Higher = more diverse. Among well-sampled breeds it ranges roughly 0.22 (least diverse) to 0.33 (most diverse).

Diversity is a strength, not a verdict on any individual dog. Lower diversity means it's worth paying attention to recessive-risk testing — not that a dog is doomed.

Cluster structure
Splits into two genetic sub-populations
Intra-breed RMS distance: 28.09 · likely working/show-line, regional, or kennel lineage split.
What does within-breed variation mean?

How much individual dogs within the breed differ from each other genetically.

How to read it: Higher = more internal variety among individuals of the breed.

Sensitive to how many dogs of the breed we've sampled.

Related breeds
Built from
Close cousins
In the Working group
Explore the full lineage map →
VBO foundation stock (breeding records) · AKC breed group
Relatedness is documented lineage + kennel family. Genetic-ancestry distance measures diversity, not kinship, so it isn't used here.
How long they live
11.2years (life expectancy)
95% CI 11–11.5 · VetCompass, McMillan 2024, n=3,531. source
What does typical lifespan mean?

The median age dogs of the breed tend to reach.

How to read it: Higher = longer-lived. Compare to longevity-for-size to see whether it's just a size effect.

Drawn from population lifespan records; individual dogs vary widely with care, genetics, and luck.

Trait genetics
Allele frequencies at named morphology loci

Frequency of the alternate allele in this breed at each locus's representative SNP.

Body size
IGF120%
HMGA21%
SMAD271%
LCORL6%
STC25%
ADAMTS1715%
Leg length
FGF4·CFA18100%
FGF4·CFA1297%
Coat
RSPO244%
FGF575%
KRT7166%
MC1R42%
Ear set
MSRB387%
Skull shape
BMP394%
SMOC277%
n = 117 dogs · high confidence · CanVAS (Brundage 2026) · Sniff Atlas
Names & origins

Other names

The Doberman Pinscher is also recorded as Doberman, Doberman Pincher, Doberman, Standard Pinscher, Dobermann, Dobie, and Dobynm.

Identified as Doberman Pinscher (VBO:0200442) in the Vertebrate Breed Ontology (Mullen et al. 2025, CC-BY 4.0) · registry IDs FCI 143 · iDog 88 · VeNom 14523.

Temperament

What Doberman Pinschers tend toward

Tendencies from owner surveys of purebred Doberman Pinschers — a leaning across the breed, not a prediction for any one dog. A bar’s strength shows how much of that behavior breed actually explains: for most it’s faint, because the rest is your dog, their training, and the life you give them.

Biddabilitybreed ~18%
biddableindependent
Human Sociabilitybreed ~11%
less sociablehighly sociable
Toy-directed Motor Patternsbreed ~18%
toy-directednot toy-directed
Environmental Engagementbreed ~9%
high engagementlow engagement
Proximity Seekingbreed ~13%
affectionatealoof
Agonistic Thresholdbreed ~9%
assertivediffident
Dog Sociabilitybreed ~8%
less sociablehighly sociable
Arousal Levelbreed ~8%
arousedcomposed
n = 37 dogs · Morrill et al. 2022, Science, Darwin's Ark (CC0)
Owner-reported purebreds; each factor n ≥ 25. "Breed ~%" is the share of this behavior explained by breed.
What you see when you look at a Doberman Pinscher

What does the genome say about how a Doberman Pinscher looks?

Doberman Pinschers look the way they do because of a small set of fixed and near-fixed morphology genes that, taken together, define the visible breed. Each translation below pairs the gene with the trait an owner actually sees, the breed's allele frequency at that locus, and a one-clause causal phrase.

Where the breed-defining genes act, mapped on a generic dog-body key — and how fixed each marker is in the Doberman Pinscher. The figure is the most-settled marker we read in that region; the full per-locus panel is below. (The silhouette is a shared anatomical guide, not this breed's outline.)

Body sizeSMAD2 · 71%Skull shapeBMP3 · 94%EarsMSRB3 · 87%Leg lengthFGF4 CFA18 · 100%Coat & colorFGF5 · 75%
CanVAS trait-locus panel (Brundage 2026)
15 morphology markers read across 5 regions. Allele frequency = how fixed a marker is in this breed, not whether your dog carries it.

Size and build

IGF1 is at 20% for the small-body allele, leaving the breed firmly in the larger end of the dog body-size spectrum.

IGF1what this gene does

IGF1 is a gene that plays a key role in determining a dog's body size. It influences how much a dog grows, affecting overall stature.

For your dog: Knowing about IGF1 gives you insight into your dog's size traits, but it’s just one part of the bigger picture when it comes to their health and care.

Full IGF1 gene page →

HMGA2 is at 1%, leaving most of the size signal to other loci in the panel.

HMGA2what this gene does

HMGA2 is a gene that influences body size in dogs, helping determine how big or small a dog grows.

For your dog: Knowing about HMGA2 helps you appreciate the genetic factors behind your dog's size, but it doesn't signal any health issues.

Full HMGA2 gene page →

SMAD2 sits at 71% at the chromosome-7 height locus.

SMAD2what this gene does

SMAD2 is a gene involved in regulating body size by influencing how cells grow and develop.

For your dog: Knowing about SMAD2 helps understand your dog's size traits but isn't linked to health issues; no immediate action needed.

Full SMAD2 gene page →

LCORL is at 6%, the NCAPG/LCORL height locus running against the breed's body-size profile here.

LCORLwhat this gene does

LCORL is a gene that influences body size in dogs. It helps determine how big or small a dog might grow.

For your dog: Knowing about LCORL helps you appreciate the genetic factors behind your dog's size, but it’s just one piece of the bigger picture when it comes to health and care.

Full LCORL gene page →

STC2 is at 5%, leaving the growth-axis signal to other loci.

ADAMTS17 is at 15%, the lower-frequency allele in this breed.

ADAMTS17what this gene does

ADAMTS17 is a gene that influences body size and also plays a role in certain eye conditions. It affects the structure of tissues in the eye and elsewhere in the body.

For your dog: If your dog belongs to a breed known to carry ADAMTS17 variants, it’s worth discussing genetic testing and eye exams with your vet to stay ahead of potential issues.

Full ADAMTS17 gene page →

Leg length

The FGF4 retrogene on chromosome 18 is near-fixed in this breed at 100%. This is the leg-length variant. The breed is fully committed to the long-legged form rather than the short-legged Corgi-and-Dachshund body plan.

The FGF4 retrogene on chromosome 12 is near-fixed at 97%, the chondrodystrophic variant associated with intervertebral disc disease risk in breeds that carry it.

Coat type, length, and color

RSPO2 sits at 44% for the furnishings variant. Furnishings (the eyebrow-and-mustache pattern seen in Schnauzers and Wheaten Terriers) vary across the population at this intermediate frequency, and visible expression depends on the specific allele combination each dog carries.

RSPO2what this gene does

RSPO2 influences the texture and appearance of a dog's coat, particularly the presence of 'furnishings' like mustaches and eyebrows. It helps determine whether a dog has that distinctive wiry or textured look.

For your dog: If your dog has those wiry eyebrows or a mustache, RSPO2 is part of the reason—no health worries, just a coat feature worth knowing about.

Full RSPO2 gene page →

FGF5 sits at 75% for the long-coat variant. Coat length is influenced by other loci as well, so intermediate FGF5 frequencies do not always correspond to intermediate visible coat lengths.

FGF5what this gene does

FGF5 is a gene that influences the length of a dog's coat. It acts like a natural switch, telling hair follicles when to stop growing longer fur.

For your dog: If your dog has a notably long or short coat, FGF5 is likely part of the reason—no action needed, but it’s a neat genetic detail to know.

Full FGF5 gene page →

KRT71 sits at 66% for the wavy/curly variant. Coat curl varies across individuals at this intermediate frequency, and visible expression is also influenced by modifier loci.

KRT71what this gene does

KRT71 is a gene that influences the curliness of a dog's coat. It helps determine whether a dog's fur is straight or has a distinctive curl.

For your dog: If your dog has a curly coat, KRT71 is likely part of the reason; it’s a natural variation, not a health concern.

Full KRT71 gene page →

MC1R sits at 42% at the representative SNP. MC1R controls the switch between red-to-gold pigment and black-to-brown pigment, with the e/e homozygous genotype producing the gold-to-red spectrum. Substrate frequencies at this SNP depend on the array's polarity, so visible coat color in the breed is a more reliable indicator than this single number.

MC1Rwhat this gene does

MC1R is a gene that influences coat color in dogs, affecting how pigments are produced in the fur.

For your dog: Knowing about MC1R gives insight into your dog's coat color but doesn't relate to health issues.

Full MC1R gene page →

Ears

MSRB3 is at 87% for the drop-ear allele, the genetic basis of the breed's signature dropped ear set.

MSRB3what this gene does

MSRB3 is a gene involved in the development of ear shape and structure in dogs.

For your dog: Understanding MSRB3 helps explain why your dog's ears look the way they do, but it isn't linked to any health issues.

Full MSRB3 gene page →

Skull shape

BMP3 is at 94%, contributing to the breed's brachycephalic skull shape.

BMP3what this gene does

BMP3 is a gene that influences the shape of a dog's skull, particularly contributing to a shorter, broader head shape known as brachycephaly.

For your dog: If your dog has a broad, short skull, it's worth discussing with your vet how this might impact their health, even though BMP3 isn't directly tied to illness.

Full BMP3 gene page →

SMOC2 sits at 77%, contributing to the breed's moderate head shape.

SMOC2what this gene does

SMOC2 influences the shape of a dog's skull, particularly affecting how flat or short the face appears.

For your dog: If your dog has a short nose, it's worth discussing with your vet how this trait might impact their health over time.

Full SMOC2 gene page →
Mendelian-disease genetics

What genetic diseases do Doberman Pinschers carry?

From a panel of 250 Mendelian-disease variants screened in 1,054,293 dogs (Donner et al. 2023), Doberman Pinschers carry 15 of them at observable frequency. Carrier frequency is not clinical risk. Most recessive variants require two copies for disease expression; many dominant variants show incomplete penetrance. Read this as a population fingerprint of what's in the gene pool, not a per-dog prediction.

n = 2,219 dogs · 2 variants tested · OMIA:000162-9615 · omia.org →
PDK4what this gene does

PDK4 helps regulate how cells use energy, especially in the heart muscle.

For your dog: If your dog is one of the breeds known to carry this gene, it’s worth discussing heart health with your vet, but being a carrier doesn’t mean your dog will develop disease.

high 36.5%
n = 2,218 dogs · 1 variant tested · OMIA:001057-9615 · omia.org →
Degenerative Myelopathy (DM)
Autosomal recessive (Incomplete penetrance)
low 0.45%
n = 2,219 dogs · 1 variant tested · OMIA:000263-9615 · omia.org →
SOD1what this gene does

SOD1 is a gene that helps protect cells from damage caused by harmful molecules called free radicals.

For your dog: If your dog is a carrier of SOD1 variants, it's worth discussing with your vet, but remember carrier status doesn't mean your dog will get the disease.

Collie Eye Anomaly (CEA)
Autosomal recessive
low 0.27%
n = 2,219 dogs · 1 variant tested · OMIA:000218-9615 · omia.org →
NHEJ1what this gene does

NHEJ1 is a gene involved in repairing breaks in DNA, helping maintain the integrity of genetic information in cells.

For your dog: If your dog belongs to one of the breeds known to carry this gene variant, it's worth discussing testing with your vet to understand any potential eye health risks.

Hyperuricosuria (HUU)
Autosomal recessive
low 0.20%
n = 2,219 dogs · 1 variant tested · OMIA:001033-9615 · omia.org →
SLC2A9what this gene does

SLC2A9 is a gene that helps regulate uric acid levels in a dog's body. It plays a role in how the kidneys handle this substance.

For your dog: If your dog is one of the breeds known to carry this gene variant, it’s worth discussing with your vet to understand any potential urinary health concerns.

Cone-Rod Dystrophy (cord1-PRA/crd4)
Autosomal recessive (Incomplete penetrance)
low 0.16%
n = 2,213 dogs · 1 variant tested · OMIA:001432-9615 · omia.org →
RPGRIP1what this gene does

RPGRIP1 is a gene involved in the function of photoreceptor cells in the eye, which help dogs see in different light conditions.

For your dog: If your dog belongs to a breed known to carry RPGRIP1 mutations, it’s worth discussing with your vet to understand the risks and monitor eye health.

n = 2,219 dogs · 1 variant tested · OMIA:001402-9615 · omia.org →
ABCB1what this gene does

ABCB1 is a gene that helps control how certain drugs are processed and cleared from a dog's body.

For your dog: If your dog is from a breed that carries this gene variant, ask your vet about medication sensitivities before giving any new drugs.

low <0.1%
n = 2,219 dogs · 3 variants tested · OMIA:000256-9615 · omia.org →
SLC3A1what this gene does

SLC3A1 is a gene that helps transport certain amino acids in the kidneys. It plays a key role in preventing the buildup of cystine, which can form stones.

For your dog: If your dog is from a breed known to carry SLC3A1 variants, it’s worth discussing cystinuria risks with your vet, especially if urinary issues arise.

n = 2,218 dogs · 1 variant tested · OMIA:002015-9615 · omia.org →
FAM20Cwhat this gene does

FAM20C is a gene that plays a key role in the mineralization of teeth, helping them develop properly and stay strong.

For your dog: If your dog is from one of these breeds, it's worth mentioning FAM20C to your vet when discussing dental care, but being a carrier doesn't mean your dog will have problems.

n = 2,219 dogs · 1 variant tested · OMIA:002244-9615 · omia.org →
SLC37A2what this gene does

SLC37A2 is a gene involved in how cells manage certain sugar molecules, which can affect bone development.

For your dog: If your dog is from a breed known to carry this gene variant, it's worth discussing with your vet, especially if you notice jaw discomfort or eating issues.

Cystinuria Type I-B (SLC7A9 p.A217T)
Autosomal recessive (Incomplete penetrance)
low <0.1%
n = 2,219 dogs · 2 variants tested · OMIA:001880-9615 · omia.org →
SLC7A9what this gene does

SLC7A9 is a gene that helps transport certain amino acids in the kidneys. It plays a role in how the body handles cystine, an amino acid that can form crystals.

For your dog: If your dog is a carrier, it’s worth discussing with your vet to monitor urinary health and catch any issues early.

Factor VII Deficiency
Autosomal recessive
low <0.1%
n = 2,219 dogs · 1 variant tested · OMIA:000361-9615 · omia.org →
F7what this gene does

The F7 gene helps produce a protein important for blood clotting, which stops bleeding when dogs get injured.

For your dog: If your dog is from a breed known to carry F7 variants, it's worth mentioning to your vet before any surgery or if you notice unusual bleeding.

Source: Donner J et al. 2023. Genetic prevalence and clinical relevance of canine Mendelian disease variants in over one million dogs. PLOS Genetics 19(2):e1010651 · Evidence: Limited (DTC ascertainment, tag-SNP proxy) · Confounding MEDIUM · License CC-BY-4.0 · Phene IDs from OMIA (Sydney School of Veterinary Science, The University of Sydney; DOI 10.25910/2AMR-PV70).
Sample size in this breed: 2,219 dogs from the Donner 2023 cohort.
Comparative oncology

Doberman Pinschers are a natural model for human cancer.

Some cancers appear in Doberman Pinschers and in people driven by the same somatically-altered genes, cohort by cohort and cited on both sides. That makes this breed part of how we understand, and one day treat, the human disease. This is not a prediction about your dog, it is a window into the biology we share.

Which Mendelian variants matter most for Doberman Pinschers?

The current Donner 2023 dataset has not identified Mendelian variants at observable carrier frequency in Doberman Pinschers. This is not the same as saying the breed is free of recessive disease. It means the atlas cohort (117 dogs) is too small to detect variants that may segregate at lower frequency in the broader population, or that the breed’s historical bottleneck has fixed certain alleles to near-homozygosity and eliminated others entirely.

The breed’s genetic structure is tight. Dobermans rank 10th of 107 ranked breeds for genetic diversity, with a mean heterozygosity of 0.235, which is low relative to the most genetically diverse breeds in the atlas. Four founder cohorts dominate the reconstruction: Momozawa (39), Hayward (25), Shannon (23), and Chen (18). That founder concentration, combined with the small atlas, means the absence of detected Mendelian variants is informative but not reassuring. A larger cohort would likely surface low-frequency recessives.

Health screening in Dobermans has historically focused on hip dysplasia, dilated cardiomyopathy, and von Willebrand disease, all of which are screened through the Orthopedic Foundation for Animals and breed-club testing programs. Until the atlas grows, breeders and owners should rely on OFA screening, cardiac evaluation (echocardiography for DCM, electrocardiography for arrhythmia), and vWF testing through established laboratories.

How should I test my Doberman Pinscher?

The breed-club recommended panel remains the foundation: OFA hip and elbow scoring, Doppler echocardiography for dilated cardiomyopathy screening (per the DPCA cardiac screening protocol, performed by a board-certified cardiologist), and von Willebrand factor antigen testing through the OFA. Genetic Mendelian panels do not yet add significant breed-specific risk stratification. Focus screening on the traits for which the OFA maintains breed statistics.

What should I feed a Doberman Pinscher?

Feeding a Doberman well means feeding around the breed’s known cardiac vulnerabilities and the management of a moderately large frame across a relatively short lifespan. Dobermans live a median 11.2 years (atlas-derived), which is typical for a large working breed. The cardiac risk, not joint disease, dominates the feeding calculus.

Dilated cardiomyopathy in Dobermans is a breed-signature condition with both genetic and dietary components. A documented susceptibility to DCM is well established in the breed, and the FDA’s 2018 advisory on diet-associated DCM flagged grain-free and pulse-heavy diets as a potential contributing factor (FDA 2018 advisory, updated 2022). The FDA’s 2018 advisory on diet-associated DCM did not isolate Dobermans as a top-reported breed the way it did Goldens, but the breed-club health community has documented cases clustering around grain-free formulations. The conservative position is a grain-inclusive, taurine-supplemented adult diet from a manufacturer with published feeding trials.

Taurine supplementation is non-negotiable. NRC 2006 sets a minimal taurine requirement, and many veterinary cardiologists recommend diets delivering at least 2,000 mg/kg taurine for meat-based formulations (NRC 2006, Nutrient Requirements of Dogs and Cats). Dobermans fed grain-free diets warrant periodic serum and whole-blood taurine measurement; target values should be discussed with your veterinary cardiologist, as consensus thresholds are not yet uniformly established.

Adult weight management matters as much as cardiac support. Dobermans are lean dogs by standard, but obesity exacerbates cardiac load and shortens the lifespan window. A diet that keeps a Doberman in the mid-range of ideal body condition (BCS 4-5 out of 9) from adulthood onward is the right target. Portion control is often more important than formula choice.

Electrolyte balance and the sodium question. Dobermans with early DCM or arrhythmia may benefit from moderate sodium restriction under cardiologist guidance; specific targets vary by case and should be set by your cardiologist. Healthy Dobermans on regular maintenance diets need not be sodium-restricted; NRC 2006 minimal is around 0.06% dry matter, and most commercial diets sit well above that. Work with your cardiologist if your dog has a murmur or documented arrhythmia.

What we don’t know

The Doberman Pinscher atlas cohort is small enough that any Mendelian-variant conclusions are provisional. A larger cohort would likely surface low-frequency recessives and allow for better phenotype-genotype mapping in the breed’s cardiac and hemostatic traits. The honest summary is that we do not yet have a genetic map of Doberman Pinschers detailed enough to guide breeding decisions at the Mendelian level.

The genetic basis of dilated cardiomyopathy in Dobermans is only partially understood. The breed carries a susceptibility that appears to interact with dietary factors, but the specific loci and the mechanism of diet-DCM interaction remain unsettled. Prospective studies in Dobermans would be high-yield, but the breed’s relatively small population and tight genetic structure complicate recruitment.

The interplay between the breed’s high founder concentration (four founders account for most of the pedigree reconstruction) and the absence of detected Mendelian variants is worth noting. It is possible that the breed has drifted into homozygosity at certain loci and away from others, creating a genetic landscape that looks different from larger, more diverse breeds. This is not proven; it is an inference from the structure of the atlas and the founder data.

Frequently asked questions about Doberman Pinschers

Are Doberman Pinschers prone to heart disease? Yes. Dilated cardiomyopathy is the breed’s most common cardiac disease and a leading cause of morbidity and mortality in Dobermans (Wess et al. 2010, J Vet Intern Med 24:1074-1083). Annual cardiac screening by echocardiography is recommended starting at age 3 to 4 years by the DPCA cardiac screening program. Some breeders and cardiologists screen earlier.

How long do Doberman Pinschers live? The atlas-derived median lifespan is 11.2 years. Some Dobermans live into their early teens; others die earlier from cardiac disease, orthopedic trauma, or cancer. The breed standard assumes a relatively short lifespan compared to smaller breeds.

What is the most common health problem in Doberman Pinschers? Dilated cardiomyopathy. Hip dysplasia and von Willebrand disease are also common and screened through the OFA and breed-club programs. No single Mendelian variant dominates the breed’s health landscape in the current dataset.

Should I do a DNA test on my Doberman Pinscher? Genetic Mendelian testing does not yet add significant breed-specific risk stratification for Dobermans. Focus on OFA screening (hip and elbow), Doppler echocardiography (DPCA cardiac screening protocol) for cardiac assessment, and von Willebrand factor antigen testing. Talk to your breeder about their screening protocol.

What is the best diet for a Doberman Pinscher? A grain-inclusive, taurine-supplemented adult formula from a manufacturer with published feeding trials. Taurine content should be at least 2,000 mg/kg for meat-based diets. Avoid grain-free and pulse-heavy formulations, which may increase cardiac risk in this breed.

Can Doberman Pinschers eat grain-free food? The breed has documented susceptibility to taurine-responsive dilated cardiomyopathy, and grain-free diets are associated with lower bioavailable taurine in some formulations. The conservative recommendation is grain-inclusive diets with verified taurine levels (2,000 mg/kg minimum).

Are Doberman Pinschers good with children? Dobermans are alert, loyal dogs often used as family and personal protection dogs. They can be excellent with children in well-socialized families. Early socialization and consistent training are essential. Supervision with young children is standard practice for any large, athletic breed.

What is the Doberman Pinscher’s typical temperament? Dobermans are intelligent, driven, and responsive to their handlers. They were bred for personal protection and have a natural wariness of strangers. With their own family, well-bred Dobermans are affectionate and eager to please. They require consistent leadership and regular mental and physical exercise.

A gift to human medicine

Doberman Pinschers are a natural model for human disease

Because the same genes cause the same conditions across species, the inherited conditions documented in Doberman Pinschers help researchers understand, and work toward treating, the human diseases they model. This is the dog advancing human medicine. The breed models the human disease; it does not have it, and this is not a prediction for your dog.

Human equivalents via OMIA → Mondo / OMIM. Model-of, not identity.
Documented in OMIA

Every condition recorded in the Doberman Pinscher

Beyond the testable carriers above, OMIA's literature catalogue records 26 genetic conditions in the Doberman Pinscher, 22 of which have a known human equivalent. This is the documented landscape across all Doberman Pinschers ever studied, not a prediction for any one dog.

Plus 8 more conditions recorded in the Doberman Pinscher in OMIA.

Online Mendelian Inheritance in Animals (OMIA); Nicholas, Tammen & Sydney Informatics Hub, DOI 10.25910/2AMR-PV70
Documented in the breed's literature is not carrier status and not a forecast for an individual dog. Human equivalents are mapped via Mondo/OMIM. Carrier frequencies (above) are the separately-measured testable subset (Donner 2023).
The data behind this page

Where every number on this page came from.

This page draws on three primary data sources. Carrier frequencies for the Mendelian section come from Donner et al. 2023 (CC-BY-4.0). We grade these data at evidence Limited because the cohort is a direct-to-consumer ascertainment, which biases toward owners who chose to test their dogs. The panel also uses tag-SNP proxies for some variants rather than direct causal-variant assays. Limited is a study-design grade, not a quality grade: the Donner cohort is the largest open canine-genotype dataset in existence and we are grateful for it. We rate the confounding MEDIUM.

Population-genetic dimensions (heterozygosity, intra-breed PCA distance, nearest neighbors, trait-locus frequencies) come from CanVAS (Brundage 2026), harmonized through the Sniff Atlas. The exact release date and verification commit are pinned at the bottom of the page so a researcher can trace a number back to a specific snapshot. The disease-gene-variant graph comes from OMIA (Online Mendelian Inheritance in Animals; Nicholas, Tammen, and the Sydney Informatics Hub at the Sydney School of Veterinary Science, The University of Sydney; retrieved April 2026, DOI 10.25910/2AMR-PV70).

What this page does not yet have. Inheritance modes and per-disease penetrance evidence from Donner 2023 are now in the structured data for every variant the panel covers. Mondo, OMIM, Ensembl, and HGNC cross-references on gene pages remain pending, they arrive in December 2026 alongside the imputed 9.67M-variant CanVAS dataset via the OMIA SQL dump absorption. Until then, gene IDs carry NCBI Gene and OMIA phene URLs only; the wider human-homolog and disease-ontology cross-reference set fills in with that release.

How to cite this page. The computed dimensions on this page are derived from the open Sniff Atlas v1.0.1 (Gehring 2026, doi:10.5281/zenodo.20566358, CC-BY 4.0). Full citation formats including BibTeX, RIS, and CITATION.cff at sniff.world/cite.

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References
  1. Donner J, Freyer J, Davison S, Anderson H, Blades M, Honkanen L, et al. (2023). Genetic prevalence and clinical relevance of canine Mendelian disease variants in over one million dogs. PLOS Genetics 19(2):e1010651. doi:10.1371/journal.pgen.1010651
  2. Brundage J, et al. (2026). CanVAS: a harmonized canine variant atlas. bioRxiv. doi:10.64898/2026.04.13.718238
  3. Nicholas, F.W., Tammen, I., & Sydney Informatics Hub. (2026). Online Mendelian Inheritance in Animals (OMIA) [dataset]. The University of Sydney. https://omia.org. doi:10.25910/2AMR-PV70 (retrieved April 2026).
Last updated
Sources: CanVAS (Brundage 2026) · Donner 2023 · OMIA