A Large‐Scale Cross‐Population Evaluation of Genetic Risk Variants for Dilated Cardiomyopathy in Dobermanns

ABSTRACT Previous studies suggest that genetic risk factors for dilated cardiomyopathy (DCM) in Dobermann dogs may differ between populations, complicating the use of genetic tests across subpopulations. Variants in pyruvate dehydrogenase kinase 4 ( PDK4 ) and titin ( TTN ) have been associated with DCM in North American Dobermanns, whereas two loci on chromosome 5 involving Protein Kinase AMP‐Activated Catalytic Subunit Alpha 2 ( PRKAA2 ) and Ring Finger Protein 207 ( RNF207 ) have been implicated in European populations. To assess the consistency of these signals across populations of Dobermanns, we harmonized and imputed genotype data from a Discovery cohort ( n  = 444) and a Replication cohort ( n  = 1771), and supplemented these with allele frequency data from a large diversity cohort ( n  = 3226) for cross‐platform analyses. We detected a shared association signal near RNF207 in affected dogs in both Europe and North America. In contrast, SNPs located in and near PDK4 and TTN variants showed no association with DCM in either population. These findings indicate that the RNF207 variant represents a shared genetic risk factor for DCM in Dobermanns across populations, and support the dog, particularly the Dobermann, as a relevant spontaneous model for RNF207‐driven DCM. The previously reported associations between PDK4 and TTN variants and DCM were not replicated in the North American Dobermann population, nor in the European Dobermann populations. Also, these results highlight the need for population‐specific validation and functional validation of identified variants where possible, before implementation of variants in genetic testing strategies.