| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs36115365 | 0.807 | 0.160 | 5 | 1313127 | upstream gene variant | G/A;C;T | snv | 7 | |||
| rs7335046 | 0.807 | 0.040 | 13 | 99389484 | downstream gene variant | G/C | snv | 0.80 | 7 | ||
| rs4911414 | 0.882 | 0.120 | 20 | 34141638 | regulatory region variant | T/G | snv | 0.73 | 5 | ||
| rs10816595 | 0.851 | 0.080 | 9 | 107947454 | regulatory region variant | A/G | snv | 0.33 | 4 | ||
| rs498136 | 0.851 | 0.080 | 11 | 69552350 | intergenic variant | A/C | snv | 0.68 | 4 | ||
| rs5759167 | 0.851 | 0.160 | 22 | 43104206 | TF binding site variant | G/T | snv | 0.40 | 4 | ||
| rs1015362 | 0.925 | 0.080 | 20 | 34150806 | regulatory region variant | C/T | snv | 0.42 | 3 | ||
| rs12029406 | 0.882 | 0.120 | 1 | 199936700 | intergenic variant | C/T | snv | 0.36 | 3 | ||
| rs12512631 | 0.882 | 0.200 | 4 | 71735614 | intergenic variant | T/C | snv | 0.35 | 3 | ||
| rs4785752 | 1.000 | 0.040 | 16 | 89968733 | upstream gene variant | A/G | snv | 0.42 | 2 | ||
| rs62389423 | 1.000 | 0.040 | 6 | 421281 | intergenic variant | G/A;T | snv | 8.5E-02 | 2 | ||
| rs1015363 | 1.000 | 0.040 | 20 | 34150529 | intergenic variant | G/A | snv | 0.69 | 1 | ||
| rs11263498 | 1.000 | 0.040 | 11 | 69567999 | TF binding site variant | T/C | snv | 0.51 | 1 | ||
| rs13097028 | 1.000 | 0.040 | 3 | 169747154 | regulatory region variant | C/T | snv | 0.38 | 1 | ||
| rs1341866 | 1.000 | 0.040 | 9 | 21771242 | regulatory region variant | T/C | snv | 0.34 | 1 | ||
| rs1485993 | 1.000 | 0.040 | 11 | 69547646 | intergenic variant | A/G | snv | 0.49 | 1 | ||
| rs2127675 | 1.000 | 0.040 | 6 | 32883073 | upstream gene variant | A/G | snv | 0.36 | 1 | ||
| rs228437 | 1.000 | 0.040 | 6 | 134577318 | intron variant | C/A;G;T | snv | 1 | |||
| rs6673928 | 1.000 | 0.040 | 1 | 206763900 | downstream gene variant | G/T | snv | 0.20 | 1 | ||
| rs6695772 | 1.000 | 0.040 | 1 | 212708597 | intergenic variant | C/G | snv | 0.58 | 1 | ||
| rs7033503 | 1.000 | 0.040 | 9 | 21799599 | upstream gene variant | T/C;G | snv | 1 | |||
| rs721970 | 1.000 | 0.040 | 20 | 33315727 | upstream gene variant | A/G | snv | 0.96 | 1 | ||
| rs1351212535 | 1.000 | 0.040 | 9 | 104831015 | missense variant | T/A | snv | 4.0E-06 | 1 | ||
| rs10231520 | 1.000 | 0.040 | 7 | 20742471 | intron variant | C/T | snv | 0.29 | 1 | ||
| rs17817117 | 1.000 | 0.040 | 7 | 20685203 | intron variant | G/C | snv | 0.29 | 1 |