| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1502593 | 1.000 | 0.040 | 10 | 100349445 | intron variant | G/A | snv | 0.34 | 3 | ||
| rs6511435 | 1.000 | 0.040 | 19 | 10103816 | upstream gene variant | T/A;C;G | snv | 1 | |||
| rs1799768 | 0.807 | 0.360 | 7 | 101126425 | upstream gene variant | -/A;C | ins | 6 | |||
| rs763351020 | 0.633 | 0.560 | 7 | 101132046 | missense variant | C/T | snv | 4.0E-06 | 35 | ||
| rs4965373 | 1.000 | 0.040 | 15 | 101272190 | non coding transcript exon variant | A/G | snv | 0.74 | 1 | ||
| rs28665122 | 0.807 | 0.240 | 15 | 101277522 | upstream gene variant | C/T | snv | 0.24 | 7 | ||
| rs778035915 | 1.000 | 0.040 | 12 | 101698057 | missense variant | A/G | snv | 3.4E-05 | 7.0E-06 | 1 | |
| rs5491 | 0.827 | 0.160 | 19 | 10274864 | missense variant | A/G;T | snv | 4.0E-06; 2.8E-02 | 6 | ||
| rs4684677 | 0.742 | 0.360 | 3 | 10286769 | missense variant | T/A | snv | 0.10 | 6.6E-02 | 13 | |
| rs696217 | 0.662 | 0.640 | 3 | 10289773 | missense variant | G/T | snv | 8.8E-02 | 7.1E-02 | 32 | |
| rs34911341 | 0.882 | 0.200 | 3 | 10289835 | missense variant | C/T | snv | 7.0E-03 | 7.3E-03 | 5 | |
| rs9514089 | 0.882 | 0.080 | 13 | 103058487 | intron variant | T/C | snv | 0.41 | 3 | ||
| rs362551 | 1.000 | 0.040 | 20 | 10314788 | intron variant | C/A;T | snv | 1 | |||
| rs2294901 | 1.000 | 0.040 | 20 | 10404855 | 3 prime UTR variant | A/G | snv | 0.14 | 1 | ||
| rs1545 | 0.925 | 0.080 | 20 | 10405365 | missense variant | C/A | snv | 0.14 | 0.14 | 2 | |
| rs1547 | 0.925 | 0.080 | 20 | 10405411 | missense variant | G/A | snv | 0.14 | 0.14 | 2 | |
| rs6133922 | 1.000 | 0.040 | 20 | 10420425 | intron variant | A/G | snv | 6.4E-02 | 1 | ||
| rs4925 | 0.677 | 0.560 | 10 | 104263031 | missense variant | C/A | snv | 0.25 | 0.23 | 28 | |
| rs6077785 | 1.000 | 0.040 | 20 | 10430806 | intron variant | A/C;T | snv | 1 | |||
| rs6108572 | 1.000 | 0.040 | 20 | 10432111 | intron variant | A/T | snv | 0.52 | 1 | ||
| rs6995374 | 1.000 | 0.040 | 8 | 10468602 | intergenic variant | C/G | snv | 0.22 | 1 | ||
| rs9282541 | 0.790 | 0.160 | 9 | 104858554 | missense variant | G/A | snv | 1.3E-02 | 4.4E-03 | 13 | |
| rs12686004 | 1.000 | 0.040 | 9 | 104891145 | intron variant | G/A | snv | 9.1E-02 | 6 | ||
| rs3905000 | 0.925 | 0.080 | 9 | 104894789 | intron variant | G/A | snv | 0.14 | 5 | ||
| rs1883025 | 0.807 | 0.120 | 9 | 104902020 | intron variant | C/T | snv | 0.28 | 13 |