Table 3B.
SNP | Chr | Physical position | Nearest gene | Feature | Major/minor allele | MAFa | Odds ratio | 95% CI | p Value | phetb |
---|---|---|---|---|---|---|---|---|---|---|
rs4987756 | 18 | 59,060,091 | BCL2 | Intron | A/G | 0.01 | 2.99 | 1.88, 4.76 | 3.78×10−6 | 0.63 |
rs1256143 | 14 | 63,981,380 | MTHFD1 | Intron | C/T | 0.19 | 1.72 | 1.21, 1.66 | 1.43×10−5 | 0.05 |
rs13004470 | 2 | 242,159,756 | BOK | Intron | C/T | 0.18 | 1.39 | 1.19, 1.62 | 4.69×10−5 | 0.81 |
rs9830448 | 3 | 154,349,978 | RAPB2 | Locus region | C/A | 0.07 | 1.58 | 1.28, 2.02 | 4.79×10−5 | 0.73 |
MAF = minor allele frequency.
p-for-heterogeneity by Cochran’s Q.