| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs42490 | 0.882 | 0.160 | 8 | 89766285 | intron variant | G/A | snv | 0.60 | 5 | ||
| rs7057398 | 0.827 | 0.080 | X | 106901299 | intron variant | T/C | snv | 0.41 | 5 | ||
| rs12008279 | 0.882 | 0.080 | X | 106917472 | intron variant | A/G;T | snv | 3 | |||
| rs12014762 | 0.882 | 0.080 | X | 106940440 | intron variant | C/T | snv | 0.14 | 3 | ||
| rs4409525 | 0.925 | 0.040 | X | 106897095 | intron variant | G/A | snv | 0.28 | 2 | ||
| rs13228878 | 1.000 | 0.040 | 7 | 142765617 | intron variant | G/A | snv | 0.51 | 1 | ||
| rs5917027 | 1.000 | 0.040 | X | 106919404 | intron variant | C/A;T | snv | 1 | |||
| rs62228256 | 1.000 | 0.040 | 20 | 51837908 | intron variant | C/T | snv | 2.7E-02 | 1 | ||
| rs4437130 | 1.000 | 0.040 | 3 | 2035283 | intergenic variant | G/A | snv | 0.12 | 2 | ||
| rs62561366 | 1.000 | 0.040 | 9 | 95555669 | intergenic variant | A/T | snv | 3.9E-02 | 2 | ||
| rs379742 | 1.000 | 0.040 | X | 106250703 | intergenic variant | G/A | snv | 0.17 | 1 | ||
| rs2995271 | 0.925 | 0.040 | 10 | 30230903 | regulatory region variant | C/T | snv | 0.64 | 2 | ||
| rs748405415 | 0.790 | 0.160 | 7 | 142773993 | stop gained | G/A;T | snv | 8 | |||
| rs199695765 | 0.925 | 0.160 | 7 | 130269008 | stop gained | C/T | snv | 8.8E-05 | 1.3E-04 | 2 | |
| rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 226 | |
| rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 223 | ||
| rs4986791 | 0.456 | 0.840 | 9 | 117713324 | missense variant | C/T | snv | 5.7E-02 | 4.9E-02 | 182 | |
| rs1051740 | 0.592 | 0.760 | 1 | 225831932 | missense variant | T/C | snv | 0.32 | 0.27 | 56 | |
| rs3775291 | 0.602 | 0.640 | 4 | 186082920 | missense variant | C/G;T | snv | 1.2E-04; 0.28 | 51 | ||
| rs17107315 | 0.620 | 0.440 | 5 | 147828115 | missense variant | T/C | snv | 9.1E-03 | 8.2E-03 | 40 | |
| rs1801725 | 0.633 | 0.600 | 3 | 122284910 | missense variant | G/T | snv | 0.13 | 0.11 | 39 | |
| rs201893408 | 0.695 | 0.480 | 8 | 93795970 | missense variant | T/A;C | snv | 8.0E-06; 1.5E-04 | 28 | ||
| rs11556218 | 0.653 | 0.600 | 15 | 81305928 | missense variant | T/G | snv | 9.6E-02 | 0.12 | 27 | |
| rs1127354 | 0.667 | 0.400 | 20 | 3213196 | missense variant | C/A;G | snv | 7.5E-02 | 26 | ||
| rs1223231582 | 0.677 | 0.280 | 7 | 142750639 | missense variant | A/G | snv | 7.0E-06 | 24 |