| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11676272 | 1.000 | 0.040 | 2 | 24918669 | missense variant | A/G | snv | 0.47 | 0.57 | 5 | |
| rs62106258 | 1.000 | 0.040 | 2 | 417167 | upstream gene variant | T/C | snv | 2.9E-02 | 5 | ||
| rs10851907 | 1.000 | 0.040 | 15 | 78623522 | upstream gene variant | G/A | snv | 0.40 | 4 | ||
| rs10048146 | 1.000 | 0.040 | 16 | 86677054 | regulatory region variant | A/G | snv | 0.17 | 3 | ||
| rs2232387 | 1.000 | 0.040 | 12 | 52433824 | missense variant | C/T | snv | 0.13 | 0.14 | 3 | |
| rs35874116 | 1.000 | 0.040 | 1 | 18854899 | missense variant | T/C | snv | 0.29 | 0.31 | 3 | |
| rs149467613 | 1.000 | 0.040 | 11 | 73232438 | intron variant | G/A | snv | 3.3E-02 | 2 | ||
| rs17032907 | 0.925 | 0.040 | 1 | 8950346 | intron variant | C/T | snv | 0.17 | 2 | ||
| rs2274328 | 0.925 | 0.040 | 1 | 8949385 | missense variant | A/C | snv | 0.49 | 0.51 | 2 | |
| rs2735733 | 1.000 | 0.040 | 11 | 1240410 | intron variant | C/T | snv | 0.49 | 0.43 | 2 | |
| rs2857476 | 1.000 | 0.040 | 11 | 1259904 | intron variant | T/C | snv | 0.54 | 2 | ||
| rs931608 | 1.000 | 0.040 | 19 | 22431320 | intron variant | A/C;T | snv | 2 | |||
| rs10180496 | 1.000 | 0.040 | 2 | 12828774 | intron variant | A/G | snv | 0.15 | 1 | ||
| rs10242311 | 1.000 | 0.040 | 7 | 105633273 | intron variant | A/C | snv | 6.2E-02 | 1 | ||
| rs10772314 | 1.000 | 0.040 | 12 | 10551751 | upstream gene variant | T/A | snv | 0.47 | 1 | ||
| rs10811723 | 1.000 | 0.040 | 9 | 22542286 | intergenic variant | A/G | snv | 0.55 | 1 | ||
| rs10987008 | 1.000 | 0.040 | 9 | 125899321 | intron variant | T/A | snv | 0.54 | 1 | ||
| rs1108343 | 1.000 | 0.040 | 16 | 51177684 | non coding transcript exon variant | T/C | snv | 0.52 | 1 | ||
| rs11166135 | 1.000 | 0.040 | 1 | 98883280 | intergenic variant | A/G | snv | 0.10 | 1 | ||
| rs1122171 | 1.000 | 0.040 | 5 | 135174297 | intron variant | C/T | snv | 0.56 | 1 | ||
| rs11672900 | 1.000 | 0.040 | 19 | 48717066 | intron variant | A/G;T | snv | 1 | |||
| rs12602978 | 1.000 | 0.040 | 17 | 27240054 | intron variant | C/T | snv | 9.3E-02 | 1 | ||
| rs1352724 | 1.000 | 0.040 | 5 | 107747786 | intergenic variant | C/A | snv | 0.15 | 1 | ||
| rs1383934 | 1.000 | 0.040 | 4 | 72551807 | intron variant | G/A | snv | 0.68 | 1 | ||
| rs140357883 | 1.000 | 0.040 | 22 | 29896823 | intron variant | T/-;TT;TTT | delins | 1 |