Human genetic basis of fulminant viral hepatitis.

Hum Genet · 2020 · PMC7153696 · PMID 32285199

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of borderline significanceno p-value reported

They found a difference of borderline significance in the distribution of the 157insMTTTVP insertion between patients and controls ( p value 0.037), with an allelic frequency of the insertion of 37% in patients and 28% in controls.

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