Barely Significant
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Pathophysiological lessons from rare associations of autoimmune diseases.

Clin Kidney J · 2012 · PMC5783216 · PMID 29497510

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highly significantno p-value reported
In patients with iMN, our GWAS study revealed a highly significant association with HLA-DQA1 alleles, with the risk of developing iMN being multiplied by 80 in individuals homozygous for the most significantly associated SNPs [ 4 ].

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