Common and Rare Variants in Genes Associated with von Willebrand Factor Level Variation: No Accumulation of Rare Variants in Swedish von Willebrand Disease Patients.

TH Open · 2020 · PMC7603419 · PMID 33145474

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highly significantno p-value reported

This difference is highly significant, and it means that the O blood group is present in 71% of individuals compared to the Swedish national average of approximately 40% (refer to Supplementary Table S1 for details on all ABO alleles and genotypes).

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