| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 4 | |
| rs429358 | 0.590 | 0.600 | 19 | 44908684 | missense variant | T/C | snv | 0.14 | 0.16 | 2 | |
| rs17107315 | 0.620 | 0.440 | 5 | 147828115 | missense variant | T/C | snv | 9.1E-03 | 8.2E-03 | 2 | |
| rs146292819 | 0.790 | 0.240 | 9 | 104794495 | missense variant | T/G | snv | 2.9E-04 | 3.8E-04 | 1 | |
| rs137852673 | 0.851 | 0.120 | 11 | 17395915 | missense variant | G/A;T | snv | 5.0E-06; 2.0E-05 | 1 | ||
| rs137852674 | 0.925 | 0.120 | 11 | 17430887 | missense variant | G/C | snv | 1 | |||
| rs72559715 | 0.827 | 0.160 | 11 | 17394379 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
| rs72559734 | 0.807 | 0.160 | 11 | 17474955 | missense variant | C/A;T | snv | 4.0E-06; 8.0E-06 | 1 | ||
| rs121917815 | 0.925 | 0.120 | 3 | 186854303 | missense variant | C/T | snv | 4.0E-06; 1.2E-05 | 1 | ||
| rs121434593 | 1.000 | 0.080 | 19 | 40237979 | missense variant | C/T | snv | 1 | |||
| rs121912706 | 0.851 | 0.200 | 4 | 113373306 | missense variant | C/T | snv | 1.0E-03 | 9.2E-04 | 1 | |
| rs7412 | 0.641 | 0.640 | 19 | 44908822 | missense variant | C/T | snv | 6.2E-02 | 7.9E-02 | 1 | |
| rs1803274 | 0.763 | 0.360 | 3 | 165773492 | missense variant | C/T | snv | 0.18 | 0.18 | 1 | |
| rs121909262 | 0.851 | 0.120 | 3 | 122254304 | missense variant | C/G;T | snv | 1 | |||
| rs777919630 | 0.623 | 0.680 | 21 | 43062358 | missense variant | G/A;T | snv | 8.0E-06; 4.0E-06 | 1 | ||
| rs104893649 | 1.000 | 0.080 | 2 | 181678529 | missense variant | C/A | snv | 1 | |||
| rs769268803 | 0.851 | 0.080 | 7 | 44147747 | missense variant | C/G;T | snv | 4.0E-06 | 1 | ||
| rs6688832 | 0.752 | 0.440 | 1 | 9263851 | missense variant | G/A;C | snv | 0.28; 1.2E-04 | 1 | ||
| rs121918673 | 0.925 | 0.200 | 17 | 37701122 | missense variant | G/C | snv | 1.9E-05 | 1 | ||
| rs137853337 | 1.000 | 0.080 | 20 | 44428409 | missense variant | G/A | snv | 8.0E-06; 8.0E-06 | 7.0E-06 | 1 | |
| rs121913150 | 1.000 | 0.080 | 19 | 7120707 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs182552223 | 1.000 | 0.080 | 19 | 7141787 | missense variant | T/C | snv | 1.2E-04 | 1.4E-05 | 1 | |
| rs267607196 | 0.827 | 0.160 | 11 | 17387248 | missense variant | C/T | snv | 2.4E-05 | 2.8E-05 | 1 | |
| rs80356610 | 0.827 | 0.080 | 11 | 17387968 | missense variant | A/G | snv | 1 | |||
| rs199472698 | 0.925 | 0.200 | 11 | 2570725 | missense variant | G/A;C | snv | 8.0E-06 | 1 |