Source: GWASDB
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10509129 | 1.000 | 0.040 | 10 | 60311283 | intron variant | G/A;T | snv | 1 | |||
| rs10761473 | 1.000 | 0.040 | 10 | 60300624 | intron variant | C/G | snv | 0.12 | 1 | ||
| rs10821736 | 1.000 | 0.040 | 10 | 60345295 | intron variant | C/T | snv | 0.12 | 1 | ||
| rs10821745 | 1.000 | 0.040 | 10 | 60376448 | intron variant | T/G | snv | 9.7E-02 | 1 | ||
| rs10821748 | 1.000 | 0.040 | 10 | 60393180 | intron variant | G/C | snv | 0.12 | 1 | ||
| rs10821789 | 1.000 | 0.040 | 10 | 60525580 | intron variant | G/A | snv | 9.2E-02 | 1 | ||
| rs10821792 | 1.000 | 0.040 | 10 | 60538858 | intron variant | C/T | snv | 8.3E-02 | 1 | ||
| rs10994308 | 1.000 | 0.040 | 10 | 60339194 | intron variant | G/A | snv | 0.12 | 1 | ||
| rs10994322 | 1.000 | 0.040 | 10 | 60376521 | intron variant | C/A;T | snv | 1 | |||
| rs10994336 | 0.776 | 0.160 | 10 | 60420054 | intron variant | C/T | snv | 7.5E-02 | 2 | ||
| rs10994338 | 0.882 | 0.040 | 10 | 60421370 | intron variant | G/A | snv | 7.5E-02 | 2 | ||
| rs10994359 | 0.827 | 0.040 | 10 | 60462349 | intron variant | T/C | snv | 8.0E-02 | 3 | ||
| rs10994397 | 0.851 | 0.040 | 10 | 60519366 | intron variant | C/T | snv | 9.5E-02 | 2 | ||
| rs10994404 | 1.000 | 0.040 | 10 | 60528687 | intron variant | T/C;G | snv | 1 | |||
| rs10994415 | 1.000 | 0.040 | 10 | 60562276 | intron variant | T/C | snv | 8.7E-02 | 1 | ||
| rs10994429 | 1.000 | 0.040 | 10 | 60611321 | intron variant | C/T | snv | 0.12 | 1 | ||
| rs10994430 | 1.000 | 0.040 | 10 | 60612195 | intron variant | G/T | snv | 0.12 | 1 | ||
| rs10994443 | 1.000 | 0.040 | 10 | 60635760 | intron variant | G/A | snv | 0.11 | 2 | ||
| rs12412135 | 1.000 | 0.040 | 10 | 60523076 | intron variant | C/T | snv | 9.2E-02 | 1 | ||
| rs12416380 | 1.000 | 0.040 | 10 | 60396396 | intron variant | A/G | snv | 9.5E-02 | 1 | ||
| rs1380459 | 1.000 | 0.040 | 10 | 60337573 | intron variant | C/T | snv | 0.12 | 1 | ||
| rs16915196 | 1.000 | 0.040 | 10 | 60600101 | intron variant | A/G | snv | 0.12 | 1 | ||
| rs16915231 | 1.000 | 0.040 | 10 | 60615288 | intron variant | G/A;T | snv | 1 | |||
| rs1938526 | 0.882 | 0.040 | 10 | 60540625 | intron variant | A/G | snv | 8.3E-02 | 2 | ||
| rs1938540 | 1.000 | 0.040 | 10 | 60535056 | intron variant | C/T | snv | 8.3E-02 | 1 |