From: Genetic variant rs17225178 in the ARNT2 gene is associated with Asperger Syndrome
SNP ID | Chromosomal position | Major/minor allele | MAF (CEU) |
---|---|---|---|
rs1446336 | 80704652 | T/A | 0.407 |
rs16972073 | 80709303 | G/C | 0.075 |
rs12594558 | 80709766 | C/T | 0.259 |
rs1026016 | 80710955 | C/T | 0.153 |
rs3910982 | 80712122 | C/A | 0.333 |
rs1020397 | 80718738 | G/C | 0.283 |
rs4778790 | 80721271 | A/G | 0.389 |
rs1912 | 80723361 | C/T | 0.138 |
rs8034535 | 80725974 | A/G | 0.208 |
rs8036233 | 80729687 | T/A | 0.474 |
rs3901896 | 80734097 | C/T | 0.394 |
rs3848173 | 80734588 | C/T | 0.129 |
rs17788120 | 80742881 | T/C | 0.411 |
rs17225178 | 80743866 | T/A | 0.081 |
rs3848175 | 80747103 | G/A | 0.281 |
rs895444 | 80749761 | A/G | 0.111 |
rs12591546 | 80754740 | G/T | 0.275 |
rs4778795 | 80760069 | G/T | 0.226 |
rs12905523 | 80760688 | T/C | 0.240 |
rs4778798 | 80770223 | T/C | 0.042 |
rs7181179 | 80778586 | T/C | 0.009 |
rs4778599 | 80781763 | G/A | 0.296 |
rs7175825 | 80795419 | G/C | 0.442 |
rs11858186 | 80801472 | C/T | 0.491 |
rs12439920 | 80804741 | G/A | 0.103 |
rs11072922 | 80806183 | C/T | 0.159 |
rs4778604 | 80837819 | C/T | 0.492 |
rs4423382 | 80854992 | A/C | 0.155 |
rs10851935 | 80859935 | T/C | 0.341 |
rs7403706 | 80861365 | T/C | 0.168 |
rs7403013 | 80874261 | G/A | 0.127 |
rs4072568 | 80884025 | G/A | 0.137 |
rs6495511 | 80888783 | A/G | 0.243 |
rs1139650 | 80889940 | A/G | 0.093 |