本研究的目的是鉴定s100a14位点的功能性基因变异体，评价其与ESCC易感性的关系。
In this study, we sought to identify functional genetic variants in the S100A14 locus and assessed their associations with susceptibility to ESCC.
评价（Valuation）：目的是确定功能点估算中包含的检查项是否该包含。
The objective deals with whether items included in the function point count should of been included.
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