| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs395998 | 1.000 | 0.040 | 1 | 196770707 | upstream gene variant | C/T | snv | 0.61 | 1 | ||
| rs402032 | 1.000 | 0.040 | 1 | 196749084 | downstream gene variant | C/G | snv | 6.5E-02 | 1 | ||
| rs4751889 | 1.000 | 0.040 | 10 | 122372672 | upstream gene variant | T/C | snv | 0.41 | 1 | ||
| rs503002 | 1.000 | 0.040 | 1 | 196851157 | intron variant | A/G | snv | 0.66 | 1 | ||
| rs6428363 | 1.000 | 0.040 | 1 | 196874581 | intron variant | G/A | snv | 0.39 | 1 | ||
| rs6428364 | 1.000 | 0.040 | 1 | 196874919 | intron variant | C/T | snv | 0.21 | 1 | ||
| rs6428365 | 1.000 | 0.040 | 1 | 196875001 | intron variant | C/A | snv | 0.21 | 1 | ||
| rs6428366 | 1.000 | 0.040 | 1 | 196875037 | intron variant | A/G | snv | 0.21 | 1 | ||
| rs6428367 | 1.000 | 0.040 | 1 | 196875062 | intron variant | T/C | snv | 0.21 | 1 | ||
| rs6428368 | 1.000 | 0.040 | 1 | 196875180 | intron variant | T/C | snv | 0.19 | 1 | ||
| rs6428369 | 1.000 | 0.040 | 1 | 196875205 | intron variant | T/C | snv | 0.23 | 1 | ||
| rs6428370 | 1.000 | 0.040 | 1 | 196875463 | intron variant | A/C;G | snv | 0.38 | 1 | ||
| rs6428379 | 1.000 | 0.040 | 1 | 196968406 | upstream gene variant | T/C | snv | 0.65 | 1 | ||
| rs6663083 | 1.000 | 0.040 | 1 | 197011530 | downstream gene variant | T/C | snv | 0.38 | 1 | ||
| rs6667243 | 1.000 | 0.040 | 1 | 196972363 | downstream gene variant | T/C | snv | 0.62 | 1 | ||
| rs6675769 | 1.000 | 0.040 | 1 | 196972531 | downstream gene variant | G/A;T | snv | 1 | |||
| rs6679884 | 1.000 | 0.040 | 1 | 196848868 | upstream gene variant | G/A;T | snv | 1 | |||
| rs6695525 | 1.000 | 0.040 | 1 | 196876391 | intron variant | T/G | snv | 0.41 | 1 | ||
| rs7412359 | 1.000 | 0.040 | 1 | 196863795 | intron variant | G/A | snv | 0.19 | 1 | ||
| rs7514704 | 1.000 | 0.040 | 1 | 196870861 | intron variant | A/G | snv | 0.22 | 1 | ||
| rs7516560 | 1.000 | 0.040 | 1 | 196870300 | intron variant | T/C | snv | 0.23 | 1 | ||
| rs7517126 | 1.000 | 0.040 | 1 | 196871142 | intron variant | A/G | snv | 0.23 | 1 | ||
| rs7517587 | 1.000 | 0.040 | 1 | 196871635 | intron variant | A/G | snv | 0.22 | 1 | ||
| rs7519492 | 1.000 | 0.040 | 1 | 196870995 | intron variant | T/C | snv | 0.22 | 1 | ||
| rs7519758 | 1.000 | 0.040 | 1 | 196856157 | intron variant | C/T | snv | 0.23 | 1 |