Table 1.
CHR | SNP | POS | Nearest Gene | Allele | OR | pValue | Ref. | Frequency | Two-tailed p value | One-tailed p value | OR | 95% CIs | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Case | Control | ||||||||||||
2 | rs17183814 | 166152389 | SCN2A | G/A | 1.142 | 2.02E−09 | 14 | 0.873 | 0.856 | 0.0623 | 0.0311 | 1.153 | 0.993-1.340 |
3 | rs2302417 | 52814256 | ITIH3 | T/A | 1.076 | 6.59E−11 | 14 | 0.609 | 0.590 | 0.144 | 0.0718 | 1.083 | 0.974-1.205 |
3 | rs3804640 | 107793709 | CD47 | A/G | 1.065 | 1.99E−08 | 14 | 0.865 | 0.848 | 0.0738 | 0.0369 | 1.147 | 0.987-1.334 |
4 | rs11724116 | 162294038 | FSTL5 | C/T | 1.088 | 2.37E−08 | 14 | 0.863 | 0.858 | 0.571 | 0.285 | 1.045 | 0.898-1.215 |
6 | rs10455979 | 166995260 | RPS6KA2 | G/C | 1.064 | 4.31E−08 | 14 | 0.703 | 0.715 | 0.336 | 0.168 | 0.944 | 0.840-1.061 |
7 | rs4236274 | 1896413 | MAD1L1 | A/G | 1.149 | 8.49E−12 | 15 | 0.478 | 0.445 | 0.0146 | 0.00731 | 1.140 | 1.026-1.266 |
7 | rs4332037 | 1950809 | MAD1L1 | T/C | 1.170 | 1.91E−09 | 17 | 0.115 | 0.097 | 0.0209 | 0.0104 | 1.218 | 1.030-1.441 |
9 | rs12553324 | 23347865 | ELAVL2 | G/C | 1.120 | 5.87E−09 | 15 | 0.498 | 0.512 | 0.297 | 0.148 | 0.946 | 0.853-1.050 |
10 | rs10821745* | 62136206* | ANK3 | G/T | 1.145 | 6.76E−09 | 14 | 0.238 | 0.236 | 0.835 | 0.418 | 1.013 | 0.896-1.145 |
10 | rs78089757 | 127112829 | intergenic | A/G | 1.410 | 3.99E−07 | 17 | 0.026 | 0.019 | 0.0881 | 0.0440 | 1.358 | 0.955-1.931 |
11 | rs174576 | 61603510 | FADS1/2 | A/C | 1.130 | 1.34E−10 | 17 | 0.457 | 0.430 | 0.0459 | 0.0229 | 1.110 | 1.002-1.230 |
11 | rs7122539 | 66662731 | RCE1 | G/A | 1.067 | 3.77E−08 | 14 | 0.517 | 0.496 | 0.113 | 0.0565 | 1.086 | 0.980-1.204 |
11 | rs12575685 | 70517927 | SHANK2 | A/G | 1.073 | 7.71E−09 | 14 | 0.278 | 0.265 | 0.285 | 0.143 | 1.066 | 0.948-1.197 |
11 | rs12290811 | 79083620 | ODZ4 | A/T | 1.190 | 7.81E−11 | 18 | 0.062 | 0.057 | 0.428 | 0.214 | 1.093 | 0.878-1.360 |
11 | rs329674 | 133776948 | LOC646543 | A/G | 1.220 | 9.59E−08 | 17 | 0.193 | 0.198 | 0.678 | 0.339 | 0.973 | 0.855-1.107 |
12 | rs10744560 | 2387099 | CACNA1C | T/C | 1.076 | 3.62E−10 | 14 | 0.060 | 0.053 | 0.287 | 0.143 | 1.130 | 0.902-1.415 |
15 | rs4447398 | 42904904 | HAUS2 | A/C | 1.099 | 9.37E−09 | 14 | 0.270 | 0.274 | 0.701 | 0.350 | 0.977 | 0.870-1.099 |
16 | rs11647445 | 9926966 | GRIN2A | G/T | 1.079 | 1.08E−10 | 14 | 0.076 | 0.076 | 0.978 | 0.489 | 1.003 | 0.826-1.217 |
17 | rs76317718 | 8222777 | ARHGEF15 | G/T | 1.190 | 2.24E−07 | 17 | 0.723 | 0.725 | 0.848 | 0.424 | 0.989 | 0.882-1.109 |
17 | rs112114764 | 42201041 | HDAC5 | G/T | 1.071 | 2.45E−08 | 14 | 0.802 | 0.790 | 0.244 | 0.122 | 1.080 | 0.949-1.229 |
20 | rs6130764 | 43750410 | STK4 | T/C | 1.064 | 3.25E−08 | 14 | 0.859 | 0.855 | 0.732 | 0.366 | 1.027 | 0.883-1.194 |
Note:
*rs10821745 is a proxy SNP for rs10994318 (r2 = 0.945 in Chinese and r2 = 1.000 in Europeans from 1000 Genomes Project), which has been reported in a previous GWAS14, and the rs10821745’s position is also shown in Table 1
The frequency and OR are based on the first allele shown in the fifth column
CHR chromosome, SNP single nucleotide polymorphism, POS position, OR odds ratio, Ref. reference, CIs confidence intervals
The significant p values (p < 0.05) were marked in bold