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Labrador DNA Health Panel

Turnaround: approx. 2 weeks

Save 34% Save 34%
Original price £149.00
Original price £149.00 - Original price £149.00
Original price £149.00
Current price £99.00
£99.00 - £99.00
Current price £99.00
  • Macular Corneal Dystrophy (MCD) 
  • Stargardt Disease (STGD) 
  • Centronuclear Myopathy (CNM)
  • Exercise-Induced Collapse (EIC)
  • Hereditary Nasal Parakeratosis (HNPK)
  • Progressive Retinal Atrophy (PRA-PRCD)
  • Skeletal Dysplasia 2 (SD2)
  • Degenerative Myelopathy (DM)
PGL UK KC (£150) CAGT (£173) Laboklin (£150)

MCD

Macular Corneal Dystrophy

STGD

Stargardt Disease

CNM

Centronuclear Myopathy

EIC

Exercise Induced Collapse

HNPK

Hereditary nasal Parakeratosis

prcd-PRA

Progressive Retinal Atrophy

SD2

Skeletal Dysplasia 2

DM

Degenerative Myelopathy

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Interpreting your results

CLEAR: No copies of the disease-causing mutation were detected

CARRIER: One copy of the disease-causing mutation was detected. The animal can pass on the disease-causing mutation to their offspring but is not considered at risk for the disease. This term is only used for autosomal recessive disorders.

AT RISK:

  • Autosomal recessive conditions: Two copies of the disease-causing mutation were detected. The animal is at risk of developing the disorder.
  • Autosomal dominant conditions: Either one or two copies of the disease-causing mutation were detected. The animal is at risk of developing the disorder. The number of copies will be listed on your test certificate.