Source: GWASDB ×
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10788994 | 1 | 55035303 | upstream gene variant | C/T | snv | 0.20 | 3 | ||||
| rs10789117 | 1 | 62606594 | intron variant | A/C;T | snv | 5 | |||||
| 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 | |||||
| rs11206510 | 0.763 | 0.240 | 1 | 55030366 | intergenic variant | T/A;C;G | snv | 7 | |||
| rs11206514 | 1 | 55050331 | intron variant | C/A | snv | 0.52 | 3 | ||||
| rs11207997 | 1 | 62596235 | intron variant | C/T | snv | 0.39 | 5 | ||||
| rs11465759 | 1 | 67166721 | intron variant | T/G | snv | 2.4E-02 | 4 | ||||
| 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 | ||||
| rs11591147 | 0.677 | 0.360 | 1 | 55039974 | missense variant | G/A;T | snv | 1.2E-02 | 4 | ||
| rs1165287 | 1 | 55054539 | intron variant | G/A | snv | 0.52 | 3 | ||||
| rs1167998 | 1 | 62465961 | intron variant | C/A | snv | 0.57 | 5 | ||||
| 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 | ||||
| rs12087003 | 1 | 94037627 | intron variant | A/G | snv | 6.3E-02 | 3 | ||||
| rs12127701 | 1 | 109295642 | intron variant | A/G | snv | 6.2E-02 | 3 | ||||
| rs12740374 | 0.851 | 0.040 | 1 | 109274968 | 3 prime UTR variant | G/T | snv | 0.22 | 8 | ||
| rs1277930 | 1 | 109279521 | downstream gene variant | G/A | snv | 0.63 | 4 | ||||
| rs1321655 | 1 | 160124668 | intron variant | A/G;T | snv | 5 | |||||
| rs17035665 | 1 | 109271097 | intron variant | C/T | snv | 0.19 | 3 | ||||
| rs17111503 | 0.925 | 0.160 | 1 | 55037775 | upstream gene variant | A/G | snv | 0.22 | 3 | ||
| rs1748197 | 1 | 62590441 | intron variant | G/A | snv | 0.42 | 5 |