| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
| rs351855 | 0.597 | 0.560 | 5 | 177093242 | missense variant | G/A | snv | 0.33 | 0.26 | 1 | |
| rs11554273 | 0.689 | 0.240 | 20 | 58909365 | missense variant | C/A;G;T | snv | 4.0E-06 | 1 | ||
| 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 | |||
| rs121913500 | 0.529 | 0.600 | 2 | 208248388 | missense variant | C/A;G;T | snv | 4.0E-06 | 1 | ||
| rs17851045 | 0.672 | 0.400 | 12 | 25227341 | missense variant | T/A;G | snv | 4.0E-06 | 1 | ||
| rs1390558952 | 1.000 | 0.040 | 6 | 149683082 | missense variant | C/T | snv | 1.4E-05 | 1 | ||
| rs104894226 | 0.658 | 0.560 | 11 | 534285 | missense variant | C/A;G;T | snv | 1 | |||
| rs104894229 | 0.564 | 0.600 | 11 | 534289 | missense variant | C/A;G;T | snv | 1 | |||
| rs104894231 | 0.776 | 0.360 | 11 | 533467 | missense variant | C/G;T | snv | 1 | |||
| rs28933406 | 0.667 | 0.480 | 11 | 533875 | missense variant | G/C;T | snv | 1 | |||
| rs200567905 | 1.000 | 0.040 | 22 | 26027116 | missense variant | G/A | snv | 1.9E-04 | 1.6E-04 | 1 | |
| rs1057519922 | 0.790 | 0.200 | 2 | 177234082 | missense variant | C/G;T | snv | 1 | |||
| rs1388363572 | 1.000 | 0.040 | 15 | 88135386 | missense variant | C/A | snv | 7.0E-06 | 1 | ||
| rs1057519925 | 0.683 | 0.560 | 3 | 179210291 | missense variant | G/A;C | snv | 1 | |||
| rs1057519927 | 0.716 | 0.240 | 3 | 179218295 | missense variant | A/C;G;T | snv | 1 | |||
| rs1057519929 | 0.776 | 0.320 | 3 | 179199066 | missense variant | G/A | snv | 1 | |||
| rs121913281 | 0.623 | 0.520 | 3 | 179234296 | missense variant | C/T | snv | 1 |