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Hemochromatosis DNA Test

$195.00

The Hemochromatosis DNA Test helps determine your risk of hereditary hemochromatosis, a condition that leads to excessive iron absorption. This test identifies the most common mutations in the HFE gene (C282Y, H63D, and S65C) associated with the condition. Early detection can empower you to make informed health and lifestyle choices to manage your risk.

  • Detect common HFE gene mutations linked to hereditary hemochromatosis.
  • Easy, at-home sample collection using a painless mouth swab.
  • Access your results securely online, with complete privacy.

Summary

Understand Your Risk of Hemochromatosis

Hemochromatosis is a hereditary condition where your body absorbs too much iron from food. This excess iron builds up, potentially damaging your organs. Common symptoms include fatigue, joint pain, and abdominal pain. Left untreated, it can lead to liver disease, heart problems, and diabetes.

Early Detection is Key

Many people with hemochromatosis don’t realize it. Symptoms are often subtle or mistaken for other conditions. But, early detection is crucial. If you have a family history of hemochromatosis, or are experiencing unexplained symptoms, it pays to know your risk.

How Does the Hemochromatosis DNA Test Work?

The DNA Family Check Hemochromatosis DNA Test identifies three mutations in the HFE gene linked to hemochromatosis:

  • C282Y: The primary mutation associated with severe symptoms of hemochromatosis, prevalent in approximately 85% of cases.
  • H63D & S65C: These mutations also contribute to hemochromatosis risk, albeit with generally milder symptoms compared to C282Y.

Hemochromatosis is inherited when you receive two mutated HFE genes, one from each parent. The highest risk is in those with two copies of the C282Y mutation. While not everyone with these genes will develop symptoms, other health factors can contribute to the condition.

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