| 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 | |||
| rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 174 | |
| rs699 | 0.501 | 0.800 | 1 | 230710048 | missense variant | A/G | snv | 0.55 | 0.58 | 134 | |
| rs1801131 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 93 | |
| rs61747728 | 0.701 | 0.240 | 1 | 179557079 | missense variant | C/T | snv | 3.0E-02 | 2.8E-02 | 20 | |
| rs121913059 | 0.716 | 0.280 | 1 | 196747245 | missense variant | C/T | snv | 1.4E-04 | 1.9E-04 | 16 | |
| rs2808630 | 0.742 | 0.240 | 1 | 159711078 | downstream gene variant | C/T | snv | 0.77 | 13 | ||
| rs6677604 | 0.827 | 0.200 | 1 | 196717788 | intron variant | G/A | snv | 0.23 | 7 | ||
| rs869025495 | 0.851 | 0.080 | 1 | 179564715 | missense variant | G/A | snv | 6 | |||
| rs758564400 | 0.925 | 0.120 | 1 | 204156683 | missense variant | A/G | snv | 4.0E-06 | 5 | ||
| rs841853 | 0.882 | 0.200 | 1 | 42935767 | intron variant | A/C | snv | 0.66 | 4 | ||
| rs11122576 | 1.000 | 0.080 | 1 | 230710933 | intron variant | T/C | snv | 8.2E-02 | 2 | ||
| rs1926723 | 1.000 | 0.080 | 1 | 230704350 | intron variant | T/A;C;G | snv | 1.2E-05; 0.11; 2.0E-05 | 2 | ||
| rs3729548 | 1.000 | 0.080 | 1 | 42934681 | intron variant | C/T | snv | 0.32 | 2 | ||
| rs11568054 | 1 | 230709809 | intron variant | G/A | snv | 3.6E-02 | 1 | ||||
| rs55807605 | 1 | 196736919 | missense variant | G/A | snv | 1.4E-03 | 5.5E-04 | 1 | |||
| rs57960694 | 1 | 196994083 | missense variant | G/A | snv | 1.1E-02 | 3.6E-02 | 1 | |||
| rs763059810 | 0.623 | 0.600 | 2 | 136115750 | missense variant | T/C | snv | 4.0E-06 | 41 | ||
| rs140511594 | 0.742 | 0.360 | 2 | 165941111 | missense variant | G/A | snv | 1.3E-04 | 1.1E-04 | 13 | |
| rs315952 | 0.763 | 0.400 | 2 | 113132727 | missense variant | T/A;C | snv | 4.0E-06; 0.31 | 10 | ||
| rs4972593 | 0.925 | 0.200 | 2 | 173598126 | intergenic variant | T/A | snv | 0.20 | 3 | ||
| rs55703767 | 0.925 | 0.160 | 2 | 227256385 | missense variant | G/A;T | snv | 4.0E-06; 0.17 | 3 | ||
| rs121912863 | 1.000 | 2 | 227008112 | missense variant | G/A | snv | 1.6E-04 | 1.8E-04 | 2 | ||
| rs1427118369 | 2 | 227283830 | missense variant | G/A | snv | 4.0E-06 | 1.4E-05 | 1 |