£115.00
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Results: ~4-6 weeks
Doctor’s report included
Convenient home or clinic sampling
Free delivery & returns
The haemochromatosis gene test analyses your DNA for specific mutations in the HFE gene, most commonly C282Y and H63D, which are associated with hereditary haemochromatosis and iron overload. It may also include checks for other related variants to assess risk of excessive iron absorption.
Sample collection: A small blood sample is taken (usually EDTA tube) by a finger-prick kit at home or in one of our UK clinics. Our kit includes everything needed; simply return the sample in the pre-paid envelope. Results include a personalised doctor’s interpretation.
Age restriction: Adults 18+ only (guardian consent required for minors).
The haemochromatosis gene test is a genetic screening blood test that identifies mutations linked to hereditary haemochromatosis, a condition causing excessive iron buildup in the body. It checks for faulty genes that can lead to iron overload in organs like the liver, heart, and pancreas, potentially causing damage. Your doctor may order this test if you have high iron levels on routine blood tests or symptoms such as fatigue, joint pain, or liver issues. The test helps confirm diagnosis, identify carriers, and assess family risk. Swift Blood Tests processes samples rapidly, with results and a doctor’s report typically within 4-6 weeks.
the primary variants tested that affect iron regulation and absorption.
determines if you have one or two faulty genes, indicating risk of symptoms or passing the condition to children.
evaluates potential for conditions like liver disease, diabetes, or heart problems due to excess iron.
A venous blood sample is required (collected in a purple-top EDTA tube). No special patient preparation (such as fasting) is needed for this genetic test. Simply drink water and eat normally unless otherwise instructed. Send samples via the next-day laboratory service.
In individuals with high serum ferritin or transferrin saturation suggesting iron overload.
For family screening if a relative is diagnosed, as it's autosomal recessive.
Of elevated iron levels, such as liver disease or alcohol misuse.
Such as those with family history or symptoms, enabling early intervention like venesection.
You may be advised to take a haemochromatosis gene test if you have any of the following signs or risk factors: - Symptoms of iron overload: Feeling very tired all the time (fatigue), joint pain, abdominal pain, skin darkening, or erectile dysfunction. - High iron on blood tests: Elevated transferrin saturation or serum ferritin from routine checks. - Family history: A close relative diagnosed with haemochromatosis or early liver/heart disease. - Unexplained liver problems: Such as abnormal liver function tests. For example, a patient with chronic fatigue and high iron levels may have HFE mutations on this test. Similarly, someone with a family history might be a carrier. Your doctor will interpret the results alongside your history and may order additional tests based on the findings.
If you can’t find the test you’re looking for, simply give us a call and our support team will guide you to the right option. We’re here to ensure you get the correct test quickly and confidently.
A haemochromatosis gene test analyses your DNA for mutations in genes like HFE that cause iron overload. It determines if you have hereditary haemochromatosis or are a carrier.
It is often ordered if you have symptoms like fatigue or joint pain, high iron levels, or a family history. It can help diagnose the condition or assess risk for relatives.
No special preparation is usually required. You can eat and drink normally. If the test is part of multiple tests, your provider will advise you.
A small blood sample is taken from a vein in your arm using a needle. It is quick (often under 5 minutes) and routine. You may feel a brief pinch; afterwards, a bandage is applied. There are minimal risks.
Risks are very low. You might experience slight pain or bruising at the needle site, which usually resolves quickly. In rare cases, a small bruise or feeling faint can occur.
Results are typically available within 4-6 weeks. Swift Blood Tests provides a detailed doctor’s report explaining your results. You will be notified by email or phone as agreed.
Yes. Swift Blood Tests offers a convenient home sample collection kit (finger-prick or small tube) with instructions, or you can choose a clinic appointment. Follow the included instructions to collect and return the sample by post.
Genetic results are not affected by diet or medications, but discuss any family history or symptoms with the doctor for accurate interpretation.
An abnormal result (e.g., two faulty genes) confirms haemochromatosis and risk of iron overload. One faulty gene means you’re a carrier. Your doctor will explain and may recommend treatment or family testing.
This test is intended for adults (18+). Children’s genetics differ, and testing minors requires specialist advice. If needed for a child, please consult with a paediatric specialist or contact us for guidance.
