| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
| rs763110 | 0.653 | 0.560 | 1 | 172658358 | upstream gene variant | C/T | snv | 0.49 | 30 | ||
| rs3219489 | 0.672 | 0.360 | 1 | 45331833 | missense variant | C/A;G | snv | 0.29 | 0.27 | 24 | |
| rs74315329 | 0.732 | 0.240 | 1 | 171636338 | stop gained | G/A | snv | 1.1E-03 | 8.7E-04 | 15 | |
| rs369410616 | 0.752 | 0.280 | 1 | 45329400 | missense variant | C/T | snv | 2.0E-05 | 2.8E-05 | 10 | |
| rs74315330 | 0.776 | 0.080 | 1 | 171636331 | missense variant | G/A | snv | 9 | |||
| rs4656461 | 0.827 | 0.040 | 1 | 165717968 | TF binding site variant | G/A | snv | 0.85 | 7 | ||
| rs199746824 | 0.807 | 0.040 | 1 | 171652139 | missense variant | C/G;T | snv | 4.0E-06; 1.6E-05 | 6 | ||
| rs566289099 | 0.807 | 0.080 | 1 | 171636310 | missense variant | G/A | snv | 2.0E-05 | 3.5E-05 | 6 | |
| rs74315328 | 0.807 | 0.120 | 1 | 171636131 | missense variant | A/G | snv | 6 | |||
| rs74315339 | 0.807 | 0.120 | 1 | 171652468 | missense variant | C/A | snv | 9.8E-04 | 1.3E-04 | 6 | |
| rs1192415 | 0.925 | 0.040 | 1 | 91611540 | TF binding site variant | G/A | snv | 0.81 | 4 | ||
| rs2234927 | 0.851 | 0.040 | 1 | 171638703 | missense variant | G/A;C | snv | 4.0E-06; 7.6E-04 | 4 | ||
| rs74315334 | 0.851 | 0.040 | 1 | 171636341 | missense variant | C/T | snv | 4 | |||
| rs74315336 | 0.851 | 0.040 | 1 | 171636173 | missense variant | T/C | snv | 4 | |||
| rs74315341 | 0.851 | 0.040 | 1 | 171636686 | missense variant | C/T | snv | 4 | |||
| rs121909194 | 0.882 | 0.040 | 1 | 171636302 | missense variant | C/G | snv | 3 | |||
| rs137853277 | 0.925 | 0.040 | 1 | 171636382 | missense variant | G/A | snv | 7.0E-04 | 3.1E-04 | 3 | |
| rs1466441587 | 0.882 | 0.040 | 1 | 107874935 | missense variant | G/A | snv | 7.0E-06 | 3 | ||
| rs2234926 | 0.882 | 0.040 | 1 | 171652385 | missense variant | C/T | snv | 0.15 | 0.11 | 3 | |
| rs2801219 | 0.882 | 0.040 | 1 | 107959790 | intron variant | C/A | snv | 0.62 | 3 | ||
| rs3766355 | 0.882 | 0.040 | 1 | 78491756 | intron variant | C/A;T | snv | 3 | |||
| rs547984 | 0.882 | 0.040 | 1 | 237933586 | intergenic variant | A/C | snv | 0.60 | 3 | ||
| rs576499843 | 0.882 | 0.040 | 1 | 107617607 | missense variant | A/C;G | snv | 8.0E-06 | 7.0E-06 | 3 |