Association analyses for FECD case/control status.
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Chr., chromosome; No. SNPs, number of SNPs in or near gene passing QC; Best SNP, SNP with smallest p value; Position, physical map position (NCBI human genome build 36); Ref. All., reference (minor) allele; OR, odds ratio per copy of the reference allele (additive model) or for presence of minor allele (dominant model). p values in italics are less than 0.05; in bold, less than 0.001. *, dominant model.
创建时间：
2015-12-02
