| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs34612342 | 0.653 | 0.400 | 1 | 45332803 | missense variant | T/C | snv | 1.5E-03 | 1.6E-03 | 11 | |
| rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 6 | |
| rs4245739 | 0.708 | 0.360 | 1 | 204549714 | 3 prime UTR variant | C/A;G | snv | 0.77; 6.2E-06 | 6 | ||
| rs11102001 | 0.925 | 0.080 | 1 | 109757069 | missense variant | G/A | snv | 9.4E-02 | 0.16 | 2 | |
| rs1218582 | 0.925 | 0.080 | 1 | 154861707 | intron variant | G/A | snv | 0.46 | 2 | ||
| rs1800871 | 0.508 | 0.800 | 1 | 206773289 | 5 prime UTR variant | A/G | snv | 0.69 | 2 | ||
| rs9651118 | 0.683 | 0.480 | 1 | 11802157 | intron variant | T/C | snv | 0.18 | 2 | ||
| rs11577139 | 1.000 | 0.080 | 1 | 98200569 | intergenic variant | C/A;T | snv | 1 | |||
| rs142173175 | 1.000 | 0.080 | 1 | 22906770 | missense variant | T/C | snv | 1.2E-03 | 4.7E-03 | 1 | |
| rs145889899 | 0.882 | 0.120 | 1 | 54010411 | splice acceptor variant | C/T | snv | 6.2E-04 | 2.4E-03 | 1 | |
| rs1800872 | 0.495 | 0.840 | 1 | 206773062 | 5 prime UTR variant | T/G | snv | 0.69 | 1 | ||
| rs1800947 | 0.683 | 0.440 | 1 | 159713648 | splice region variant | C/A;G;T | snv | 4.4E-05; 5.1E-02; 4.0E-06 | 1 | ||
| rs1801131 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 1 | |
| rs201754821 | 1.000 | 0.080 | 1 | 22784861 | missense variant | G/A | snv | 8.8E-05 | 3.5E-05 | 1 | |
| rs35882952 | 1.000 | 0.080 | 1 | 22863060 | missense variant | G/C;T | snv | 4.0E-06; 1.1E-03 | 1 | ||
| rs372653137 | 1.000 | 0.080 | 1 | 22910526 | missense variant | A/G | snv | 4.0E-05 | 1.8E-04 | 1 | |
| rs486907 | 0.667 | 0.360 | 1 | 182585422 | missense variant | C/T | snv | 0.31 | 0.28 | 1 | |
| rs636291 | 0.925 | 0.080 | 1 | 10496040 | intron variant | G/A | snv | 0.55 | 1 | ||
| rs76826147 | 0.882 | 0.080 | 1 | 22913757 | stop gained | A/G;T | snv | 4.2E-06; 2.9E-03 | 1 | ||
| rs121913500 | 0.529 | 0.600 | 2 | 208248388 | missense variant | C/A;G;T | snv | 4.0E-06 | 19 | ||
| rs9282858 | 0.716 | 0.320 | 2 | 31580756 | missense variant | C/T | snv | 1.8E-02 | 2.1E-02 | 7 | |
| rs1800440 | 0.653 | 0.440 | 2 | 38070996 | missense variant | T/C;G | snv | 0.15; 4.0E-06 | 6 | ||
| rs4988235 | 0.752 | 0.400 | 2 | 135851076 | intron variant | G/A;C | snv | 4 | |||
| rs721048 | 0.851 | 0.200 | 2 | 62904596 | intron variant | G/A | snv | 0.13 | 4 | ||
| rs12621278 | 0.790 | 0.280 | 2 | 172446825 | intron variant | A/G | snv | 4.9E-02 | 3 |