Table 2B.
SNP | Chr | Physical position | Nearest gene | Feature | Major/minor allele |
MAFa | Odds ratio | 95% CI | p Value | phetb |
---|---|---|---|---|---|---|---|---|---|---|
rs11088283 | 21 | 34,745,649 | KCNE1 | Intron | A/G | 0.47 | 0.85 | (0.78, 0.93) | 4.88×10−5 | 0.09 |
rs3745274 | 19 | 46,204,681 | CYP2B6 | Coding, non-synonymous | G/T | 0.24 | 1.24 | (1.12, 1.38) | 4.99×10−5 | 0.01 |
rs12428227 | 13 | 109,700,293 | COL4A1 | Intron | A/G | 0.17 | 1.23 | (1.10, 1.38) | 5.20×10−5 | 0.14 |
rs17151901 | 8 | 10,290,865 | MSRA | Intron | C/T | 0.02 | 1.36 | (1.09, 1.69) | 6.53×10−5 | 0.01 |
MAF = minor allele frequency.
p-for-heterogeneity by Cochran’s Q.