Given this context, interpreting the results poses challenges due to the risk of overgeneralizing aspects that, in reality, may be more nuanced and pertain specifically to oculocutaneous albinism type 1 (OCA1) or type 2 (OCA2), ocular albinism (OA), or Hermansky-Pudlak syndrome (HPS) for example. The gene discussed is TYR; the disease is ocular albinism.