TABLE II.
GWAS Results of Significant SNPs Associated With Sensory Gating
| CHR | Location (BP) | SNPs | BETA | SE | P-value | Risk allele |
Ref. allele |
Risk allele frequency |
INFO | Genotyped |
|---|---|---|---|---|---|---|---|---|---|---|
| 14 | 85615940 | rs10149105 | 20.1793 | 3.3717 | 5.12E-09 | T | C | 0.2212 | 1.0503 | Yes |
| 14 | 85617384 | rs10132223 | 21.3939 | 3.4342 | 1.27E-09 | T | G | 0.2072 | 1.056 | No |
| 14 | 85617393 | rs10144282 | −20.0177 | 3.3748 | 6.90E-09 | T | G | 0.7783 | 1.0475 | No |
| 14 | 85617703 | chr14_85617703_I* | 20.0052 | 3.375 | 7.06E-09 | GT | G | 0.2217 | 1.0473 | No |
| 14 | 85618302 | rs10135204 | 19.8278 | 3.3937 | 1.13E-08 | T | C | 0.2202 | 1.0409 | No |
| 14 | 85618459 | rs10147584 | −19.9705 | 3.3506 | 5.87E-09 | T | C | 0.7698 | 1.032 | No |
| 14 | 85619165 | rs9652388 | 19.9258 | 3.3752 | 8.06E-09 | A | G | 0.2216 | 1.0474 | No |
| 14 | 85619232 | rs7157801 | 19.9104 | 3.4278 | 1.36E-08 | C | G | 0.2158 | 1.021 | No |
| 14 | 85619625 | rs7158211 | 19.826 | 3.3742 | 9.39E-09 | T | C | 0.2216 | 1.0482 | No |
INFO, imputation quality score.
Genomic positions are in UCSC hg19/NCBI Build 37.
*
Chr14_85617703_I is a GT vs. G insertion variant.