Sample report
A full example of the report you'll receive, same layout and depth. Juno's breed mix and markers are real lab output; the other sections show representative example values.
Complete Dog DNA Test
Juno's report
Sample · example report
Meet Juno.
A Foxhound-forward mix with a more typical background, a family-loving temperament, and a clean read on the wellness markers we screened.
Who is Juno?
The breed mix, the coat, and the temperament their genes lean toward.
Breed mix
Led by American Foxhound.
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Coat
Tricolour, non-merle, full pigment.
- Base colour
- Tricolour
- Pattern
- Tan points with white
- Dilution
- None (full pigment)
- White markings
- Minor white markings possible
- Merle
- Non-merle
MC1R (E) and ASIP (A) are N-masked in canFam4; a commercial coat test is recommended for those.
Pigment-lightening modifier
IRF4 change may lighten pigment (links to the Copy Number panel).
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- E (MC1R) e/?: N-masked in canFam4; a commercial coat test resolves this best.
- K (CBD103) ky/ky: Allows the A-locus pattern to show.
- A (ASIP) ay/?: Sable possible.
- B (TYRP1) B: Black eumelanin, not brown.
- D (MLPH) D: Full pigment, not dilute.
- M (PMEL) m: Non-merle.
Temperament & traits
Breed-informed leanings, not a measurement of Juno's individual personality.
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Wellness
Markers and lineage, framed as things to know, never a diagnosis.
Known markers
We screened 479 sites. 359 came back clear. The markers worth knowing about are below.
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Genetic diversity
More diverse than about 12% of dogs.
Inbreeding coefficient 31.4% versus a panel median of 23.8% (1,929 dogs). Lower is a more diverse, more outbred background.
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The deep science
The heavy genomics, summarized calmly. Open any of them for the full readout.
ChromosomesAll balanced
What this means: we checked that every chromosome is present in the normal amount, nothing extra, nothing missing. Everything came back balanced, which is what you want to see.
How we measured it: read depth normalised per 1 Mb window across every chromosome, mean ratio 0.999 (1.0 is a normal two-copy result), with 0 windows low and 0 high across 124 windows.
Copy numberNo copy-number changes detected
What this means: we looked for stretches of DNA that are duplicated or missing compared with other dogs. Nothing notable stood out.
How we measured it: 4-dog reference panel aligned to canFam4. A loss is confirmed when only this dog is depleted.
Rare variants2,497 high-impact catalogued
What this means:these are rare spellings in your dog's DNA that are uncommon across the wider dog population. We catalogue them for completeness. Most are harmless, and none of this is a diagnosis.
| Gene | Effect | Zygosity | Pop. freq |
|---|---|---|---|
| IGF2BP2 | Splice acceptor | hom | 0.26% |
| PLEKHG5 | Stop gained | hom | 0.9% |
| ADGRV1 | Splice donor | het | 1.4% |
How we measured it: Imputation against the Dog10K panel (29M SNPs, 1,929 dogs) with functional effect annotation.
Showing a sample; the full table filters here.
See your own dog's real report.
One cheek swab, about 4 to 5 weeks, and a report just like this one, built from your dog's actual DNA.