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Diagnosis of genetic predisposition to hemochromatosis - evaluation of 2 mutations H63D and C282Y - testing at the collection point

Diagnosis of genetic predisposition to hemochromatosis - evaluation of 2 mutations H63D and C282Y - testing at the collection point

Diagnosis of genetic predisposition to hemochromatosis - evaluation of 2 mutations H63D and C282Y

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from PLN 630.00

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Test description
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Hemochromatosis is one of the most common disease entities with a genetic basis. It is a metabolic disorder that causes increased absorption of iron from supplied food. Diagnosis of the 2 most common mutations of the HFE gene:

c.187C>G / p.His63Asp
c.845G>A / p.Cys282Tyr