| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs387907272 | 0.572 | 0.520 | 3 | 38141150 | stop lost | T/C | snv | 5.2E-05 | 7.0E-06 | 73 | |
| rs76992529 | 0.653 | 0.560 | 18 | 31598655 | missense variant | G/A | snv | 1.1E-03 | 4.9E-03 | 36 | |
| rs9344 | 0.653 | 0.480 | 11 | 69648142 | splice region variant | G/A | snv | 0.45 | 0.39 | 34 | |
| rs121909612 | 0.807 | 0.160 | 4 | 154585795 | missense variant | T/A | snv | 4.0E-06 | 7.0E-06 | 6 | |
| rs4487645 | 0.882 | 0.200 | 7 | 21898622 | intron variant | C/A;T | snv | 3 | |||
| rs10799599 | 1.000 | 0.120 | 1 | 19968007 | upstream gene variant | C/G | snv | 0.33 | 1 | ||
| rs7820212 | 1.000 | 0.120 | 8 | 52506268 | intergenic variant | T/A | snv | 0.58 | 1 | ||
| rs1005300 | 1.000 | 0.120 | 22 | 39151886 | intron variant | C/G | snv | 0.68 | 1 | ||
| rs10507419 | 1.000 | 0.120 | 13 | 34612315 | intron variant | T/A | snv | 0.22 | 1 | ||
| rs6752376 | 1.000 | 0.120 | 2 | 6303084 | intron variant | C/T | snv | 0.39 | 1 | ||
| rs79419269 | 1.000 | 0.120 | 7 | 151239990 | intron variant | T/C | snv | 7.5E-04 | 1 |