Table 2 of Yoshida, Mol Vis 2013; 19:2321-2329.
SNP | Position on chromosome five (Build 37.1) | Gene location | Alleles | Risk allele | Risk allele frequency | P | Pc | OR (95%CI) | |
---|---|---|---|---|---|---|---|---|---|
Cases (n=433) | Controls (n=542) | ||||||||
rs10462070 | 44,305,749 | Intron 2 | A/G | A | 0.901 | 0.849 | 6.5×10−4 | 0.0059 | 1.62 (1.22–2.13) |
rs12517396 | 44,359,526 | Intron 1 | A/C | C | 0.900 | 0.845 | 3.9×10−4 | 0.0030 | 1.64 (1.25–2.16) |
rs339501 | 44,365,633 | Intron 1 | A/G | A | 0.900 | 0.845 | 3.9×10−4 | 0.0030 | 1.64 (1.25–2.16) |