| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11646692 | 1.000 | 0.040 | 16 | 81238301 | upstream gene variant | C/G | snv | 0.38 | 1 | ||
| rs142408232 | 1.000 | 0.040 | 4 | 165484478 | missense variant | C/G;T | snv | 1.2E-05; 3.8E-04 | 1 | ||
| rs4690821 | 1.000 | 0.040 | 4 | 165484432 | synonymous variant | C/T | snv | 6.2E-02 | 4.5E-02 | 1 | |
| rs4264 | 1.000 | 0.040 | 7 | 93886765 | 3 prime UTR variant | C/A;T | snv | 1 | |||
| rs59805398 | 1.000 | 0.040 | 7 | 93891949 | intron variant | G/C | snv | 0.27 | 1 | ||
| rs2855262 | 1.000 | 0.040 | 4 | 24800354 | 3 prime UTR variant | T/C | snv | 0.50 | 1 | ||
| rs34489123 | 1.000 | 0.040 | 7 | 93889174 | synonymous variant | C/T | snv | 5.8E-02 | 5.9E-02 | 1 | |
| rs376307381 | 0.925 | 0.080 | 11 | 44067827 | missense variant | G/C | snv | 4.0E-06 | 2 | ||
| rs533450458 | 0.925 | 0.120 | 8 | 90042781 | missense variant | C/T | snv | 5.5E-04 | 7.7E-05 | 2 | |
| rs884164 | 0.925 | 0.040 | 19 | 4521613 | upstream gene variant | A/G;T | snv | 2 | |||
| rs2870463 | 0.882 | 0.040 | 16 | 75216819 | upstream gene variant | G/A | snv | 0.14 | 3 | ||
| rs383830 | 0.882 | 0.040 | 5 | 100613278 | intergenic variant | A/T | snv | 0.76 | 3 | ||
| rs532997003 | 0.882 | 0.040 | 9 | 104840464 | missense variant | T/C | snv | 2.0E-05 | 3 | ||
| rs428785 | 0.882 | 0.040 | 21 | 26844276 | missense variant | C/A;G;T | snv | 1.3E-05; 0.70 | 0.78 | 3 | |
| rs756140607 | 0.882 | 0.040 | 12 | 111790509 | missense variant | G/A | snv | 8.0E-06 | 3 | ||
| rs3760908 | 0.882 | 0.040 | 19 | 4184515 | intron variant | A/G | snv | 0.18 | 3 | ||
| rs200340021 | 0.925 | 0.080 | 12 | 14882204 | missense variant | C/T | snv | 7.0E-06 | 3 | ||
| rs61839258 | 0.882 | 0.040 | 10 | 18400709 | 5 prime UTR variant | G/A;C;T | snv | 0.14 | 3 | ||
| rs371150372 | 0.882 | 0.040 | 2 | 27223972 | missense variant | G/A;T | snv | 2.8E-05; 4.0E-06 | 3 | ||
| rs763172697 | 0.882 | 0.040 | 2 | 27233526 | missense variant | G/T | snv | 4.0E-06 | 3 | ||
| rs778916575 | 0.882 | 0.040 | 2 | 27222595 | missense variant | G/A | snv | 1.2E-05 | 3 | ||
| rs12704673 | 0.882 | 0.040 | 7 | 93525009 | intron variant | A/G;T | snv | 0.27 | 3 | ||
| rs138760780 | 0.882 | 0.040 | 1 | 205515245 | intron variant | C/T | snv | 1.5E-02 | 3 | ||
| rs141383962 | 0.882 | 0.040 | 8 | 27605112 | missense variant | C/G;T | snv | 7.2E-05 | 1.0E-04 | 3 | |
| rs565470 | 0.882 | 0.040 | 13 | 110186299 | intron variant | A/G | snv | 0.68 | 3 |