| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs115357105 | 0.925 | 0.080 | 9 | 104376689 | intergenic variant | A/G | snv | 1.5E-02 | 4 | ||
| rs79246196 | 0.925 | 0.080 | 7 | 100185286 | intron variant | C/T | snv | 1.8E-02 | 4 | ||
| rs12180309 | 0.925 | 0.080 | 6 | 91209048 | intergenic variant | C/T | snv | 1.9E-02 | 4 | ||
| rs9282858 | 0.716 | 0.320 | 2 | 31580756 | missense variant | C/T | snv | 1.8E-02 | 2.1E-02 | 7 | |
| rs74745534 | 1.000 | 0.080 | 6 | 49589080 | intergenic variant | C/T | snv | 2.1E-02 | 3 | ||
| rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 34 | |
| rs1867877 | 1.000 | 0.080 | 11 | 18705901 | missense variant | T/C | snv | 3.5E-02 | 4.2E-02 | 3 | |
| rs1800973 | 0.827 | 0.320 | 12 | 69350234 | missense variant | C/A | snv | 4.2E-02 | 4.3E-02 | 6 | |
| rs62313897 | 1.000 | 0.080 | 4 | 90215590 | intron variant | G/A | snv | 4.4E-02 | 3 | ||
| rs115460205 | 1.000 | 0.080 | 4 | 161890417 | intron variant | C/T | snv | 4.7E-02 | 3 | ||
| rs17536732 | 1.000 | 0.080 | 4 | 161903214 | intron variant | G/T | snv | 4.7E-02 | 3 | ||
| rs17028719 | 1.000 | 0.080 | 1 | 5734948 | intergenic variant | A/G | snv | 4.8E-02 | 1 | ||
| rs139438618 | 0.882 | 0.080 | 7 | 84008281 | intron variant | A/G | snv | 5.2E-02 | 4 | ||
| rs72716801 | 1.000 | 0.080 | 8 | 127636481 | non coding transcript exon variant | G/T | snv | 5.5E-02 | 3 | ||
| rs2066702 | 0.882 | 0.080 | 4 | 99307860 | missense variant | G/A | snv | 1.5E-02 | 5.9E-02 | 3 | |
| rs7607774 | 1.000 | 0.080 | 2 | 236520511 | intergenic variant | G/A | snv | 7.4E-02 | 1 | ||
| rs2133896 | 0.925 | 0.080 | 12 | 99455122 | intron variant | G/T | snv | 7.6E-02 | 5 | ||
| rs1869324 | 1.000 | 0.080 | 2 | 137469872 | intron variant | G/A | snv | 7.9E-02 | 1 | ||
| rs6778524 | 1.000 | 0.080 | 3 | 16814451 | intron variant | T/C | snv | 8.3E-02 | 1 | ||
| rs9458121 | 1.000 | 0.080 | 6 | 161101446 | non coding transcript exon variant | A/G | snv | 8.4E-02 | 1 | ||
| rs11558538 | 0.695 | 0.400 | 2 | 138002079 | missense variant | C/T | snv | 1.0E-01 | 8.4E-02 | 1 | |
| rs6443238 | 1.000 | 0.080 | 3 | 9407371 | intron variant | C/T | snv | 8.4E-02 | 1 | ||
| rs11922615 | 1.000 | 0.080 | 3 | 9416623 | intron variant | A/G | snv | 8.4E-02 | 1 | ||
| rs61776290 | 1.000 | 0.080 | 1 | 10634850 | upstream gene variant | C/T | snv | 8.7E-02 | 3 | ||
| rs4699741 | 1.000 | 0.080 | 4 | 99357540 | upstream gene variant | T/C | snv | 9.2E-02 | 3 |