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Genetic Haemochromotosis

£129

Genetic Haemochromotosis

Description:

Detection of polymorphisms p.His63Asp, p.Ser65Cys and p.Cys282Tyr in the HFE gene associated with Haemochromatosis. Confirmatory diagnostic genetic testing to diagnose or rule out HH should be carried out for symptomatic individuals with biochemical evidence of iron overload.

Gene List:

HFE - The HFE gene is like your body's iron gatekeeper. It controls how much iron gets absorbed from your food and stored in your body. Imagine it as a security guard at a storage facility for iron. The normal HFE gene ensures that your body has enough iron for its important functions but not too much that it becomes harmful to you. The following Variations of this gene are mutations and have the following effects:

  • C282Y: This is the most common variation and can significantly mess up the instructions. It might tell the guard to let in way too much iron.

  • H63D and S65C: These are less common variations and may cause milder confusion, potentially leading to a smaller increase in iron absorption.

Turnaround times:

Turnaround Time: 

  • 7 Days


Note:

This service is only available to the age of 16 and above.


Furthermore, Any Cancellation within 48 hours prior to appointment will incur a charge of 20% of total service cost.




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