| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3774372 | 1.000 | 0.160 | 3 | 41835922 | missense variant | T/C | snv | 0.17 | 0.18 | 4 | |
| rs7372217 | 1.000 | 0.160 | 3 | 41948630 | intron variant | G/A | snv | 0.68 | 4 | ||
| rs7651190 | 1.000 | 0.160 | 3 | 41724463 | intron variant | A/G | snv | 0.33 | 4 | ||
| rs1716983 | 1.000 | 0.160 | 3 | 41922636 | intron variant | G/A;C;T | snv | 3 | |||
| rs1717027 | 1.000 | 0.160 | 3 | 41946428 | intron variant | T/A;C | snv | 3 | |||
| rs34562254 | 1.000 | 0.160 | 17 | 16939677 | missense variant | G/A | snv | 0.14 | 0.12 | 3 | |
| rs73081364 | 1.000 | 0.160 | 3 | 41872124 | intron variant | G/A;C;T | snv | 3 | |||
| rs7622665 | 1.000 | 0.160 | 3 | 41929251 | intron variant | T/C | snv | 0.67 | 3 | ||
| rs879882 | 1.000 | 0.160 | 6 | 31171675 | intron variant | T/C;G | snv | 3 | |||
| rs10936601 | 1.000 | 0.160 | 3 | 169810661 | intron variant | C/T | snv | 0.37 | 2 | ||
| rs12630450 | 1.000 | 0.160 | 3 | 169762416 | downstream gene variant | A/G | snv | 0.33 | 2 | ||
| rs2272007 | 1.000 | 0.160 | 3 | 41954644 | missense variant | T/C | snv | 0.79 | 0.67 | 2 | |
| rs2683696 | 1.000 | 0.160 | 3 | 41873406 | intron variant | T/C | snv | 0.34 | 2 | ||
| rs28581706 | 1.000 | 0.160 | 3 | 41829905 | intron variant | A/C;T | snv | 2 | |||
| rs3821383 | 1.000 | 0.160 | 3 | 169772158 | upstream gene variant | A/C;G;T | snv | 2 | |||
| rs62258655 | 1.000 | 0.160 | 3 | 41890838 | intron variant | G/A | snv | 0.11 | 2 | ||
| rs6768542 | 1.000 | 0.160 | 3 | 41823982 | intron variant | G/A;C | snv | 2 | |||
| rs6768972 | 1.000 | 0.160 | 3 | 3180101 | upstream gene variant | A/C;G | snv | 2 | |||
| rs7193541 | 1.000 | 0.160 | 16 | 74630845 | missense variant | T/C | snv | 0.37 | 0.43 | 2 | |
| rs756168629 | 1.000 | 0.160 | 2 | 140841050 | missense variant | C/T | snv | 4.8E-05 | 1.4E-05 | 2 | |
| rs7633750 | 1.000 | 0.160 | 3 | 169791456 | upstream gene variant | G/A | snv | 0.38 | 2 | ||
| rs9856633 | 1.000 | 0.160 | 3 | 41972358 | upstream gene variant | A/G | snv | 0.68 | 2 | ||
| rs1006752 | 1.000 | 0.160 | 2 | 25441122 | intron variant | C/T | snv | 0.12 | 1 | ||
| rs1016669 | 1.000 | 0.160 | 3 | 41852948 | intron variant | T/C | snv | 0.32 | 1 | ||
| rs10180663 | 1.000 | 0.160 | 2 | 25410373 | intron variant | T/A;C;G | snv | 1 |