Gribskovens Etta

Genetic Diversity
• Heterozygosity: 38.54%
• High genetic diversity

Coat Colour & Characteristics
• Black & Rust
• Black pigment (B/B)
• Does not carry brown (liver)
• Does not carry dilution (blue/Isabella)
• Normal pigmentation
• Short coat
• No furnishing gene
• No curly coat gene

Breed-Specific Health Results
• Chondrodystrophy (CDDY / IVDD Risk): N/CDDY
• Chondrodysplasia (CDPA): N/N (Clear)
• Degenerative Myelopathy (DM): N/N (Clear)
• Progressive Retinal Atrophy (prcd-PRA): N/N (Clear)
• Charcot-Marie-Tooth Neuropathy (CMT): N/N (Clear)
• Hyperuricosuria (HUU): N/N (Clear)
• von Willebrand Disease Type I (vWD1): N/N (Clear)
• Persistent Müllerian Duct Syndrome (PMDS): N/N (Clear)
• Myotonia Congenita: N/N (Clear)
• Malignant Hyperthermia (MH): N/N (Clear)
• Comma Defect (Spondylocostal Dysostosis): N/N (Clear)

Additional Results
• Clear for tested cystinuria variants
• Clear for tested epilepsy-associated variants
• Clear for all other breed-specific variants included in the testing panel

DNA Information
• Premium SNP DNA Profile (ISAG 2020)
• DNA Profile Verified
• Blood sample collected and identity verified by licensed veterinarian Natali Zyskind (6436)
• Tested and certified by LABOKLIN GmbH & Co. KG, Germany
• Genetic identity confirmed through SNP-based DNA profiling

Breeding Summary
Fenya carries one copy of the CDDY variant (N/CDDY), associated with chondrodystrophy and an increased risk of IVDD. She is clear for all other tested breed-specific hereditary diseases and demonstrates high genetic diversity with a heterozygosity score of 38.54%.

All genetic testing was performed by LABOKLIN using a veterinarian-verified blood sample, providing a high level of confidence in the accuracy of both the DNA profile and health screening results.