| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913399 | 0.724 | 0.200 | 3 | 41224612 | missense variant | G/A;C | snv | 1 | |||
| rs121913407 | 0.763 | 0.240 | 3 | 41224645 | missense variant | T/C;G | snv | 1 | |||
| rs121913409 | 0.708 | 0.400 | 3 | 41224646 | missense variant | C/A;G;T | snv | 1 | |||
| rs121913412 | 0.724 | 0.280 | 3 | 41224633 | missense variant | A/C;G;T | snv | 1 | |||
| rs28931589 | 0.695 | 0.240 | 3 | 41224613 | missense variant | G/A;C;T | snv | 1 | |||
| rs147001633 | 0.776 | 0.240 | 2 | 25234373 | missense variant | C/A;G;T | snv | 4.0E-06; 4.0E-06; 2.2E-04 | 1 | ||
| rs377577594 | 0.827 | 0.240 | 2 | 25234374 | missense variant | G/A;C;T | snv | 1.2E-04; 8.0E-06 | 1 | ||
| rs1216460058 | 1.000 | 0.040 | 7 | 6046097 | missense variant | C/T | snv | 1 | |||
| rs1057520012 | 1.000 | 0.040 | 4 | 65404419 | missense variant | C/T | snv | 1 | |||
| rs199614818 | 1.000 | 0.040 | 4 | 65490529 | missense variant | C/A;T | snv | 4.0E-06; 2.4E-05 | 1 | ||
| rs121913469 | 0.763 | 0.240 | 17 | 39723966 | missense variant | TT/CC | mnv | 1 | |||
| rs186305118 | 1.000 | 0.040 | 17 | 64055926 | missense variant | A/C | snv | 1.0E-02; 6.8E-06 | 1.0E-02 | 1 | |
| rs758691941 | 1.000 | 0.040 | 7 | 151077331 | missense variant | C/A;T | snv | 4.1E-06; 4.1E-06 | 1 | ||
| rs1057519895 | 0.724 | 0.240 | 4 | 152328232 | missense variant | C/A;G;T | snv | 1 | |||
| rs121913482 | 0.630 | 0.680 | 4 | 1801837 | missense variant | C/T | snv | 4 | |||
| rs351855 | 0.597 | 0.560 | 5 | 177093242 | missense variant | G/A | snv | 0.33 | 0.26 | 1 | |
| rs121913495 | 0.672 | 0.400 | 20 | 58909366 | missense variant | G/A;T | snv | 2 | |||
| rs11554273 | 0.689 | 0.240 | 20 | 58909365 | missense variant | C/A;G;T | snv | 4.0E-06 | 1 | ||
| rs104894230 | 0.564 | 0.600 | 11 | 534288 | missense variant | C/A;G;T | snv | 2 | |||
| rs121913233 | 0.627 | 0.520 | 11 | 533874 | missense variant | T/A;C;G | snv | 1 | |||
| rs121917759 | 0.790 | 0.480 | 11 | 533466 | missense variant | G/A | snv | 1 | |||
| rs121913499 | 0.605 | 0.520 | 2 | 208248389 | missense variant | G/A;C;T | snv | 2 | |||
| rs121913500 | 0.529 | 0.600 | 2 | 208248388 | missense variant | C/A;G;T | snv | 4.0E-06 | 1 | ||
| rs77375493 | 0.458 | 0.760 | 9 | 5073770 | missense variant | G/A;T | snv | 3.5E-04 | 3 | ||
| rs121913530 | 0.583 | 0.640 | 12 | 25245351 | missense variant | C/A;G;T | snv | 5 |