Table 2.
SNP | Chr. position (Build 37.3) | Major/minor allele | Risk allele | Cases (n = 3410) | Controls (n = 3412) | OR for risk allele (95% CI) | P value for risk allele | OR for genotype (95% CI) | P value for genotype (empirical P value) | ||
---|---|---|---|---|---|---|---|---|---|---|---|
Risk allele frequencies | Genotype count 11/12/22# |
Risk allele frequencies | Genotype count 11/12/22# |
||||||||
rs1951867 | 54407192 | G/C | G | 0.903 | 2748/586/35 | 0.896 | 2673/617/36 | 1.073 (0.959, 1.201) | 0.220 | 1.071 (0.957, 1.198) | 0.233 |
rs7146040 | 54407920 | A/G | G | 0.097 | 2755/586/36 | 0.096 | 2768/572/38 | 1.017 (0.908, 1.140) | 0.767 | 0.983 (0.878, 1.101) | 0.769 |
rs4444235 | 54410919 | T/C | C | 0.459 | 996/167/717 | 0.452 | 1034/1593/716 | 1.026 (0.959, 1.098) | 0.461 | 0.975 (0.912, 1.043) | 0.465 |
rs17563 | 54417522 | T/C | T | 0.720 | 1800/1319/273 | 0.717 | 1733/1375/269 | 1.042 (0.967, 1.124) | 0.280 | 1.042 (0.967, 1.123) | 0.283 |
rs2071047 | 54418411 | C/T | T | 0.368 | 1380/1522/485 | 0.355 | 1428/1527/444 | 1.056 (0.985, 1.133) | 0.126 | 0.948 (0.885, 1.016) | 0.131 |
rs2761887 | 54425052 | C/A | A | 0.519 | 793/1675/920 | 0.511 | 795/1674/866 | 1.033 (0.965, 1.105) | 0.348 | 0.968 (0.905, 1.036) | 0.348 |
rs8014071 | 54431500 | A/G | G | 0.350 | 1426/1572/404 | 0.341 | 1462/1539/386 | 1.039 (0.968, 1.115) | 0.290 | 0.962 (0.896, 1.033) | 0.287 |
rs8014363 | 54431575 | T/C | T | 0.884 | 2617/690/45 | 0.873 | 2574/774/45 | 1.108 (0.999, 1.229) | 0.051 | 1.110 (1.000, 1.231) | 0.050 (0.3689) |
rs7141785 | 54433114 | C/T | C | 0.904 | 2740/572/36 | 0.902 | 2727/594/32 | 1.028 (0.916, 1.154) | 0.639 | 1.022 (0.912, 1.146) | 0.705 |
rs6572927 | 54433390 | T/A | T | 0.633 | 1345/1534/456 | 0.632 | 1327/1533/455 | 1.008 (0.940, 1.082) | 0.816 | 1.008 (0.939, 1.081) | 0.834 |
P values <0.1 were shown in bold.
The additive model was used in the association analyses between genotype and type 2 diabetes.
#11: major allele homozygotes; 12: heterozygotes; 22: minor allele homozygotes. Empirical P values are for the alleles based on 10,000 permutations.