| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
| rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
| rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 57 | ||
| rs11030101 | 0.763 | 0.160 | 11 | 27659197 | 5 prime UTR variant | A/T | snv | 0.36 | 10 | ||
| rs1805502 | 0.790 | 0.200 | 12 | 13561247 | 3 prime UTR variant | A/G | snv | 0.25 | 7 | ||
| rs2769605 | 0.827 | 0.040 | 9 | 85297756 | intergenic variant | C/T | snv | 0.44 | 5 | ||
| rs951436 | 0.925 | 0.040 | 1 | 163063552 | regulatory region variant | A/C | snv | 0.42 | 3 | ||
| rs1387923 | 0.882 | 0.040 | 9 | 85025721 | 3 prime UTR variant | A/G | snv | 0.47 | 3 | ||
| rs1565445 | 0.882 | 0.040 | 9 | 85002156 | intron variant | G/A | snv | 0.74 | 3 | ||
| rs2254137 | 0.925 | 0.040 | 2 | 207579304 | intron variant | C/A | snv | 0.57 | 2 | ||
| rs7603001 | 0.925 | 0.040 | 2 | 184902089 | intron variant | A/G;T | snv | 2 | |||
| rs7665833 | 1.000 | 0.040 | 4 | 130459962 | intergenic variant | G/A | snv | 0.11 | 1 | ||
| rs2133402 | 1.000 | 0.040 | 3 | 214575 | intron variant | T/G | snv | 0.10 | 1 | ||
| rs1516340 | 1.000 | 0.040 | 3 | 195392 | intron variant | C/A;T | snv | 1 | |||
| rs242999 | 1.000 | 0.040 | 22 | 34109914 | intron variant | T/A;C | snv | 1 | |||
| rs7735612 | 1.000 | 0.040 | 5 | 169082727 | intron variant | T/C | snv | 0.33 | 1 | ||
| rs3817629 | 1.000 | 0.040 | 11 | 237312 | intron variant | T/C | snv | 0.80 | 1 | ||
| rs12564480 | 1.000 | 0.040 | 1 | 241666284 | intron variant | T/C | snv | 0.16 | 1 | ||
| rs1841915 | 1.000 | 0.040 | 3 | 21573947 | intron variant | G/C | snv | 0.69 | 1 |