Source: GWASDB
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11819869 | 1.000 | 0.040 | 11 | 46539130 | intron variant | C/T | snv | 0.27 | 1 | ||
| rs12574668 | 1.000 | 0.040 | 11 | 46401136 | intron variant | C/A | snv | 0.22 | 1 | ||
| rs7112229 | 1.000 | 0.040 | 11 | 46491699 | intron variant | C/T | snv | 0.19 | 1 | ||
| rs7130141 | 1.000 | 0.040 | 11 | 46478324 | intron variant | C/T | snv | 0.27 | 1 |