| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6698843 | 0.925 | 0.080 | 1 | 109264212 | synonymous variant | C/A;T | snv | 4.0E-06; 0.44 | 5 | ||
| rs9436735 | 1 | 65419378 | upstream gene variant | C/G | snv | 2.5E-02 | 5 | ||||
| rs11206517 | 1.000 | 0.120 | 1 | 55060755 | intron variant | T/C;G | snv | 4 | |||
| rs11465759 | 1 | 67166721 | intron variant | T/G | snv | 2.4E-02 | 4 | ||||
| rs12127701 | 1 | 109295642 | intron variant | A/G | snv | 6.2E-02 | 4 | ||||
| rs1277930 | 1 | 109279521 | downstream gene variant | G/A | snv | 0.63 | 4 | ||||
| rs17111684 | 1 | 55159875 | intron variant | C/T | snv | 3.8E-02 | 4 | ||||
| rs17646665 | 1.000 | 0.080 | 1 | 109369429 | intron variant | A/G | snv | 5.8E-02 | 4 | ||
| rs2479409 | 1.000 | 0.040 | 1 | 55038977 | upstream gene variant | G/A | snv | 0.66 | 4 | ||
| rs3832016 | 1 | 109275536 | 3 prime UTR variant | -/T | ins | 0.74 | 4 | ||||
| rs567279 | 1 | 66222346 | intron variant | G/T | snv | 0.97 | 4 | ||||
| rs585362 | 1 | 109247173 | upstream gene variant | C/G;T | snv | 4 | |||||
| rs6657811 | 1 | 109264661 | intron variant | A/C;T | snv | 4.0E-06; 0.10 | 4 | ||||
| rs734359 | 1 | 41480231 | intron variant | C/T | snv | 7.5E-02 | 4 | ||||
| rs10788994 | 1 | 55035303 | upstream gene variant | C/T | snv | 0.20 | 3 | ||||
| rs10858082 | 1 | 109256099 | intron variant | G/A | snv | 0.48 | 3 | ||||
| rs10888898 | 1 | 55050835 | intron variant | A/G | snv | 0.59 | 3 | ||||
| rs10916704 | 1 | 20074498 | intron variant | G/A;T | snv | 3 | |||||
| rs11206514 | 1 | 55050331 | intron variant | C/A | snv | 0.52 | 3 | ||||
| rs11573244 | 1 | 20081089 | intron variant | C/T | snv | 6.6E-03 | 3 | ||||
| rs11577931 | 1 | 109278262 | downstream gene variant | A/G | snv | 5.5E-02 | 3 | ||||
| rs1165287 | 1 | 55054539 | intron variant | G/A | snv | 0.52 | 3 | ||||
| rs11806129 | 1 | 94016821 | intron variant | A/G;T | snv | 3 | |||||
| rs11806638 | 1 | 55052487 | intron variant | C/A;G | snv | 3 | |||||
| rs12027135 | 1 | 25449242 | intron variant | A/T | snv | 0.50 | 3 |