Association analyses for FECD severity grade (worse eye).

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; effect, expected change in FECD grade 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 (the Bonferroni threshold for study-wide significance at the 0.05 level). *, dominant model.