In contrast, extending SNP inclusion to the genome-wide nominally significant variants substantially improved predictive accuracy [ 47 ].
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Unveiling Novel Traits Associated with Ulcerative Colitis via Phenome-Wide Associations Enhanced by Polygenic Risk Statistics.
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This was followed by three Crohn’s disease phenotypes that nearly reached significance, including Crohn’s disease of the small intestine (K50.00), Crohn’s disease (K50.90), and Crohn’s disease of both the small and large intestine with fistula (K50.813).