Source: GWASDB
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10275045 | 0.882 | 0.160 | 7 | 1881190 | intron variant | C/T | snv | 0.35 | 3 | ||
| rs10226475 | 1.000 | 0.040 | 7 | 2186527 | intron variant | A/G | snv | 0.34 | 1 | ||
| rs12666575 | 1.000 | 0.040 | 7 | 1964786 | intron variant | C/G;T | snv | 1 | |||
| rs6461049 | 1.000 | 0.040 | 7 | 1977810 | intron variant | C/T | snv | 0.56 | 1 |