Source: GWASDB ×
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11568607 | 17 | 50668426 | splice region variant | G/A | snv | 7.4E-03 | 2.6E-02 | 4 | |||
| rs11568746 | 9 | 99105926 | intron variant | C/G | snv | 2.1E-05 | 6 | ||||
| rs11569302 | 20 | 46118465 | intron variant | C/G;T | snv | 4 | |||||
| rs11569321 | 20 | 46122724 | missense variant | C/T | snv | 1.0E-02 | 4.1E-02 | 3 | |||
| rs11570255 | 1.000 | 20 | 59300861 | missense variant | G/A;T | snv | 3.3E-03; 2.9E-05 | 6 | |||
| rs11571151 | 11 | 101127486 | missense variant | C/G;T | snv | 6 | |||||
| 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 | ||||
| rs11668319 | 19 | 19185066 | intron variant | A/G | snv | 0.15 | 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 | |||||
| rs11867309 | 17 | 55762788 | intron variant | G/A | snv | 3.3E-02 | 3 | ||||
| rs11868655 | 17 | 5522873 | intron variant | T/C | snv | 2.3E-02 | 3 | ||||
| rs11902417 | 2 | 20976028 | intergenic variant | G/A | snv | 0.25 | 7 | ||||
| rs11920918 | 3 | 196368689 | intron variant | G/A | snv | 8.5E-03 | 3 | ||||
| rs11921179 | 3 | 129976195 | intron variant | G/A | snv | 0.96 | 5 | ||||
| rs12027135 | 1 | 25449242 | intron variant | A/T | snv | 0.50 | 3 | ||||
| rs12087003 | 1 | 94037627 | intron variant | A/G | snv | 6.3E-02 | 3 | ||||
| rs12113155 | 7 | 151607887 | intron variant | A/C;G | snv | 3 | |||||
| rs12127701 | 1 | 109295642 | intron variant | A/G | snv | 6.2E-02 | 3 | ||||
| rs12248199 | 10 | 82032473 | intron variant | G/A | snv | 4.0E-02 | 3 | ||||
| rs12258934 | 10 | 82015079 | intron variant | T/C | snv | 5.1E-02 | 4 | ||||
| rs12269156 | 10 | 6470618 | intron variant | A/G | snv | 3.4E-02 | 3 |