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

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

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

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Test description

Hemochromatosis is one of the most common disease entities with a genetic basis. It is a metabolic disease 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

Receipt of results by e-mail

To receive test results electronically, it is necessary to enter the Patient's mobile number in the appropriate field in the Test Order.

This will allow the Patient to receive the results through the Synevo Online portal available at: results.synevo.pl.

After the results are released on the Synevo Online Platform, the Patient will receive an individual access code via SMS to the indicated cell phone number.

Patient will receive an individual access code via SMS

In order to log in to Synevo Online, you must go to results.synevo.pl and enter your PESEL number and the one-time access code received by SMS.

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