Source: GWASCAT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs964184 | 0.716 | 0.440 | 11 | 116778201 | 3 prime UTR variant | G/C | snv | 0.82 | 35 | ||
| rs2266788 | 0.763 | 0.440 | 11 | 116789970 | 3 prime UTR variant | G/A | snv | 0.93 | 6 | ||
| rs2075290 | 0.882 | 0.160 | 11 | 116782580 | intron variant | C/G;T | snv | 5 | |||
| rs6589566 | 0.882 | 0.080 | 11 | 116781707 | intron variant | G/A;C;T | snv | 5 | |||
| rs2075291 | 0.752 | 0.400 | 11 | 116790676 | missense variant | C/A;T | snv | 6.4E-03; 4.0E-06 | 4 | ||
| rs11604424 | 11 | 116780399 | intron variant | C/G;T | snv | 3 | |||||
| rs12286037 | 1.000 | 0.040 | 11 | 116781491 | intron variant | C/T | snv | 0.11 | 3 | ||
| rs2160669 | 1.000 | 0.040 | 11 | 116776891 | 3 prime UTR variant | C/T | snv | 0.92 | 3 | ||
| rs3741298 | 11 | 116786845 | intron variant | C/T | snv | 0.73 | 3 | ||||
| rs11823543 | 11 | 116778419 | 3 prime UTR variant | G/A | snv | 0.11 | 2 | ||||
| rs603446 | 1.000 | 0.040 | 11 | 116783719 | intron variant | C/T | snv | 0.33 | 2 | ||
| rs35120633 | 11 | 116784884 | missense variant | G/A;C | snv | 6.6E-02; 8.0E-06 | 1 | ||||
| rs75198898 | 11 | 116779090 | intron variant | G/A | snv | 7.2E-03 | 4.3E-03 | 1 |