Barely Significant

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highly significantqualifiedgold
Though the homozygously mutated genotype of FN298674 :g.90T>C significantly increases the risk of a cow to be affected by LDA and is the most likely causal SNP due to its effect on a transcription factor binding site, FN298674 :g.1891insG within the first intron of MLN also showed a highly significant association with LDA.