| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
| rs77375493 | 0.458 | 0.760 | 9 | 5073770 | missense variant | G/A;T | snv | 3.5E-04 | 187 | ||
| rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 174 | |
| rs1188383936 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 102 | ||
| rs899127658 | 0.547 | 0.720 | 11 | 46739084 | missense variant | G/A;C | snv | 82 | |||
| rs751377893 | 0.574 | 0.680 | 1 | 169546513 | missense variant | T/C | snv | 4.0E-06 | 65 | ||
| rs6025 | 0.637 | 0.560 | 1 | 169549811 | missense variant | C/T | snv | 1.8E-02 | 43 | ||
| rs763351020 | 0.633 | 0.560 | 7 | 101132046 | missense variant | C/T | snv | 4.0E-06 | 35 | ||
| rs552953108 | 0.724 | 0.200 | 11 | 46729529 | missense variant | G/A | snv | 1.6E-05 | 4.2E-05 | 16 | |
| rs747418061 | 0.807 | 0.200 | 5 | 112828920 | missense variant | G/A | snv | 3.2E-05 | 7.0E-06 | 10 | |
| rs1312546120 | 0.807 | 0.160 | 1 | 169541191 | missense variant | T/C | snv | 4.0E-06 | 7 | ||
| rs777692567 | 0.827 | 0.200 | 8 | 42182845 | missense variant | G/A | snv | 4.0E-05 | 1.4E-05 | 5 | |
| rs1371086615 | 0.851 | 0.120 | 5 | 112828890 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 4 | |
| rs765557332 | 0.851 | 0.120 | 5 | 112835075 | missense variant | G/A | snv | 7.0E-06 | 4 | ||
| rs878853423 | 0.851 | 0.120 | 5 | 112837663 | missense variant | G/A | snv | 4 | |||
| rs118203907 | 0.882 | 0.080 | 1 | 169530805 | missense variant | T/C | snv | 1.6E-05 | 1.4E-05 | 3 | |
| rs6009 | 1.000 | 0.080 | 1 | 169529596 | intron variant | T/A;C | snv | 0.94 | 3 | ||
| rs6427196 | 1.000 | 0.080 | 1 | 169511985 | 3 prime UTR variant | C/G;T | snv | 3 | |||
| rs16860992 | 1.000 | 0.080 | 3 | 186676249 | intron variant | G/C;T | snv | 3 | |||
| rs9898 | 0.925 | 0.160 | 3 | 186672838 | missense variant | C/T | snv | 0.38 | 0.43 | 3 | |
| rs2228243 | 1.000 | 0.080 | 3 | 186677324 | missense variant | A/G;T | snv | 0.20; 4.0E-06 | 3 | ||
| rs1482856709 | 0.925 | 0.080 | 3 | 93900887 | missense variant | G/A | snv | 3 | |||
| rs1431515214 | 0.925 | 0.080 | 5 | 112839790 | missense variant | G/A | snv | 4.0E-06 | 2 | ||
| rs118203906 | 0.925 | 0.080 | 1 | 169555299 | missense variant | C/G | snv | 2.3E-04 | 7.7E-05 | 2 |