| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 24 | ||
| rs7903146 | 0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv | 16 | |||
| rs11191580 | 0.827 | 0.040 | 10 | 103146454 | intron variant | T/C | snv | 7.9E-02 | 10 | ||
| rs17514846 | 0.882 | 0.120 | 15 | 90873320 | intron variant | C/A;G | snv | 5 | |||
| rs4129585 | 1.000 | 0.040 | 8 | 142231572 | intron variant | A/C | snv | 0.68 | 4 | ||
| rs12561919 | 1.000 | 0.040 | 1 | 11779866 | missense variant | C/T | snv | 0.13 | 0.13 | 3 |