Common conditions associated with hereditary haemochromatosis genetic variants: cohort study in UK Biobank.

BMJ · 2019 · PMC6334179 · PMID 30651232

Europe PMC DOI

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nominally significantno p-value reported

Given the nominally significant p.C282Y homozygote association with excess mortality (when combining men and women, aged 40 to 70 at baseline) during follow-up, we undertook post hoc analyses on causes of death.

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