Source: GWASDB
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6795970 | 0.807 | 0.200 | 3 | 38725184 | missense variant | A/G | snv | 0.65 | 0.70 | 2 | |
| rs6798015 | 1.000 | 0.080 | 3 | 38757345 | intron variant | C/T | snv | 0.70 | 2 | ||
| rs10428132 | 0.925 | 0.120 | 3 | 38736063 | intron variant | T/G | snv | 0.67 | 1 | ||
| rs10428168 | 1.000 | 0.080 | 3 | 38738568 | intron variant | T/C | snv | 0.41 | 1 | ||
| rs11129801 | 1.000 | 0.080 | 3 | 38708884 | intron variant | A/G | snv | 0.71 | 1 | ||
| rs12638572 | 1.000 | 0.080 | 3 | 38746306 | intron variant | A/G;T | snv | 1 | |||
| rs6599240 | 1.000 | 0.080 | 3 | 38697226 | 3 prime UTR variant | G/A | snv | 0.44 | 1 | ||
| rs6599257 | 1.000 | 0.080 | 3 | 38763097 | intron variant | C/T | snv | 0.74 | 1 | ||
| rs7428167 | 1.000 | 0.080 | 3 | 38736700 | intron variant | T/C | snv | 0.59 | 1 | ||
| rs7430439 | 1.000 | 0.080 | 3 | 38762148 | intron variant | G/A | snv | 0.66 | 1 | ||
| rs7641844 | 1.000 | 0.080 | 3 | 38760760 | intron variant | A/G | snv | 0.33 | 0.31 | 1 | |
| rs9874633 | 1.000 | 0.080 | 3 | 38730503 | intron variant | A/G | snv | 0.38 | 1 |