| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs213210 | 0.742 | 0.240 | 6 | 33208047 | upstream gene variant | A/C;G | snv | 11 | |||
| rs11150038 | 0.790 | 0.080 | 16 | 78042662 | intron variant | A/C;G | snv | 10 | |||
| rs17102823 | 0.776 | 0.080 | 14 | 34894698 | intergenic variant | A/C;G | snv | 10 | |||
| rs863225311 | 0.827 | 0.120 | 5 | 112819347 | splice region variant | A/C;G | snv | 7 | |||
| rs5273 | 0.827 | 0.080 | 1 | 186674636 | missense variant | A/C;G | snv | 4.0E-06; 7.6E-03 | 1.4E-02 | 6 | |
| rs9365723 | 0.827 | 0.080 | 6 | 158014540 | intron variant | A/C;G | snv | 0.56 | 5 | ||
| rs11986055 | 0.882 | 0.080 | 8 | 42277660 | intron variant | A/C;G | snv | 3 | |||
| rs9347683 | 0.882 | 0.120 | 6 | 162728023 | 5 prime UTR variant | A/C;G | snv | 3 | |||
| rs2076485 | 1.000 | 0.080 | 6 | 29556175 | missense variant | A/C;G | snv | 4.1E-06; 0.25 | 1 | ||
| rs854560 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 113 | ||
| rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
| rs2228570 | 0.521 | 0.760 | 12 | 47879112 | start lost | A/C;G;T | snv | 0.63 | 99 | ||
| rs121913274 | 0.645 | 0.320 | 3 | 179218304 | missense variant | A/C;G;T | snv | 33 | |||
| rs1799977 | 0.662 | 0.440 | 3 | 37012077 | missense variant | A/C;G;T | snv | 0.23 | 28 | ||
| rs35767 | 0.763 | 0.360 | 12 | 102481791 | upstream gene variant | A/C;G;T | snv | 13 | |||
| rs35107139 | 0.776 | 0.080 | 14 | 53952388 | intron variant | A/C;G;T | snv | 11 | |||
| rs17217772 | 0.790 | 0.240 | 2 | 47410107 | missense variant | A/C;G;T | snv | 5.8E-03 | 10 | ||
| rs4768903 | 0.790 | 0.080 | 12 | 50651666 | intron variant | A/C;G;T | snv | 9 | |||
| rs1989969 | 0.827 | 0.120 | 12 | 47884227 | intron variant | A/C;G;T | snv | 0.60 | 8 | ||
| rs314277 | 0.925 | 0.080 | 6 | 104959787 | intron variant | A/C;G;T | snv | 6 | |||
| rs63750449 | 0.925 | 0.120 | 3 | 37047640 | missense variant | A/C;G;T | snv | 3.5E-03; 8.4E-05 | 2 | ||
| rs556554798 | 1.000 | 0.080 | 12 | 20916077 | missense variant | A/C;G;T | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs2032582 | 0.538 | 0.800 | 7 | 87531302 | missense variant | A/C;T | snv | 0.54; 3.8E-02 | 97 | ||
| rs699947 | 0.570 | 0.680 | 6 | 43768652 | upstream gene variant | A/C;T | snv | 67 | |||
| rs7041 | 0.576 | 0.800 | 4 | 71752617 | missense variant | A/C;T | snv | 0.52; 4.0E-06 | 64 |