Non-HFE TFR2 (Type 3) Genetic Haemochromatosis

Although this form of the condition is considered rare, increasing levels of genetic testing for this variant are revealing more people at risk of the condition, particularly in combination with a type 1 (HFE) mutation to either C282Y, H63D or S65C genes.

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TFR2 (type 3) Non-HFE Genetic Haemochromatosis