Table 2.
SNP ID | Frequency Minor Allele (cases) | Frequency Minor Allele (controls) | OR | X 2 | Pvalue |
---|---|---|---|---|---|
rs237885 | 0.4612 | 0.458 | 1.013 | 0.0074 | 0.9317 |
rs2268490 | 0.1282 | 0.1382 | 0.9171 | 0.1535 | 0.6952 |
rs2268493 | 0.2155 | 0.3074 | 0.619 | 7.442 | 0.00637 |
rs2254298 | 0.0862 | 0.1284 | 0.6404 | 3.062 | 0.0802 |
rs53576 | 0.3559 | 0.3037 | 1.267 | 2.308 | 0.1287 |
rs237894 | 0.3248 | 0.267 | 1.321 | 2.992 | 0.0837 |
rs2268496 | 0.2179 | 0.2437 | 0.8648 | 0.6625 | 0.4157 |
rs237900 | 0.3846 | 0.3897 | 0.9787 | 0.0199 | 0.8879 |
rs2301261 | 0.0769 | 0.1078 | 0.6899 | 1.9 | 0.1681 |
Significant P values after Bonferroni correction for total number of SNPs are written in bold and italicized. AS, Asperger Syndrome; OR, odds ratio; SNP, single nucleotide polymorphism.