Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic cancer risk in Chinese populations
|Study ID||Alternative Stable ID||Type|
Study Datasets 1 dataset.
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The illumina exome chip genotyping data for 943 PDAC cases and 3,908 controls in the Chinese population. Genotypes were called by the Illumina GenomeStudio software, and the selected variants were re-called by zCall. Standard quality control were performed.