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Albinism - Siamese Overview

Albinism - Siamese
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Category: Trait (Associated with Phenotype)

Gene: TYR

Variant Detected: Deletion

Severity: Scale 2 has a low degree of severity. It has mild effects and generally does not pose any significant health concerns, or is easily managed.

Mode of Inheritance: Autosomal Recessive

Test Overview: Albinism is a congenital disorder that is characterized by lack of pigment in hair, skin and eyes.

Research Citation(s): Anim Genet. 2006 Apr; 37(2): 175–178.

Associated Breed(s): Siamese,