| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11556218 | 0.653 | 0.600 | 15 | 81305928 | missense variant | T/G | snv | 9.6E-02 | 0.12 | 27 | |
| rs1051740 | 0.592 | 0.760 | 1 | 225831932 | missense variant | T/C | snv | 0.32 | 0.27 | 56 | |
| rs17107315 | 0.620 | 0.440 | 5 | 147828115 | missense variant | T/C | snv | 9.1E-03 | 8.2E-03 | 40 | |
| rs886037774 | 0.882 | 0.120 | 8 | 19955993 | missense variant | T/C | snv | 7 | |||
| rs7057398 | 0.827 | 0.080 | X | 106901299 | intron variant | T/C | snv | 0.41 | 5 | ||
| rs74571530 | 0.882 | 0.160 | 7 | 117559594 | missense variant | T/A;C;G | snv | 9.4E-04 | 3 | ||
| rs201893408 | 0.695 | 0.480 | 8 | 93795970 | missense variant | T/A;C | snv | 8.0E-06; 1.5E-04 | 28 | ||
| rs698 | 0.724 | 0.240 | 4 | 99339632 | missense variant | T/A;C | snv | 0.35 | 20 | ||
| rs10273639 | 0.776 | 0.280 | 7 | 142749077 | upstream gene variant | T/A;C | snv | 9 | |||
| rs397508139 | 0.882 | 0.160 | 7 | 117540237 | missense variant | T/A;C | snv | 4.0E-06; 4.0E-06 | 3 | ||
| rs1451011538 | 0.925 | 0.080 | 16 | 84838647 | missense variant | T/A | snv | 4.0E-06 | 2 | ||
| rs267606982 | 0.742 | 0.120 | 7 | 142751938 | missense variant | GC/AT | mnv | 11 | |||
| rs756271986 | 0.925 | 0.040 | 7 | 142773430 | missense variant | GC/AT | mnv | 2 | |||
| rs1801725 | 0.633 | 0.600 | 3 | 122284910 | missense variant | G/T | snv | 0.13 | 0.11 | 39 | |
| rs3809849 | 0.882 | 0.120 | 17 | 4555303 | missense variant | G/C;T | snv | 0.21; 3.1E-05 | 3 | ||
| rs1801726 | 0.732 | 0.280 | 3 | 122284985 | missense variant | G/C | snv | 0.95 | 0.92 | 13 | |
| rs1800076 | 0.763 | 0.200 | 7 | 117509093 | missense variant | G/A;T | snv | 1.5E-02; 8.0E-06 | 10 | ||
| rs748405415 | 0.790 | 0.160 | 7 | 142773993 | stop gained | G/A;T | snv | 8 | |||
| rs11971167 | 0.882 | 0.160 | 7 | 117642528 | missense variant | G/A;T | snv | 1.3E-03 | 3 | ||
| rs199422123 | 0.925 | 0.040 | 7 | 142751934 | missense variant | G/A;T | snv | 2.0E-05 | 2 | ||
| rs34708521 | 1.000 | 0.040 | 5 | 35670201 | missense variant | G/A;T | snv | 0.10; 4.0E-06 | 1 | ||
| rs199769221 | 0.790 | 0.280 | 7 | 142751920 | missense variant | G/A;C;T | snv | 8.0E-05; 4.0E-06 | 8 | ||
| rs771803303 | 0.882 | 0.160 | 20 | 38148005 | missense variant | G/A;C;T | snv | 1.6E-05; 4.1E-06 | 3 | ||
| rs118204057 | 0.732 | 0.400 | 8 | 19954222 | missense variant | G/A;C | snv | 1.9E-04 | 16 | ||
| rs145844329 | 0.882 | 0.120 | 8 | 143215486 | missense variant | G/A;C | snv | 2.5E-05; 8.5E-04 | 3 |