Germline Variants Associated with Nasopharyngeal Carcinoma Predisposition Identified through Whole-Exome Sequencing.

For example, some of the variants and genes from previous NPC studies were present in our cohorts but failed to reach statistical significance ( p < 0.05), perhaps due to an insufficient sample size.

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This variant was also detected in an independent validation cohort but did not reach statistical significance.

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