| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913530 | 0.583 | 0.640 | 12 | 25245351 | missense variant | C/A;G;T | snv | 5 | |||
| rs121913273 | 0.605 | 0.440 | 3 | 179218294 | missense variant | G/A;C | snv | 5 | |||
| rs121913483 | 0.649 | 0.560 | 4 | 1801841 | missense variant | C/A;G;T | snv | 4.2E-06; 1.3E-05 | 4 | ||
| rs104886003 | 0.562 | 0.440 | 3 | 179218303 | missense variant | G/A;C | snv | 4.0E-06 | 4 | ||
| rs121918502 | 0.790 | 0.160 | 10 | 121517351 | missense variant | G/C | snv | 3 | |||
| rs121434592 | 0.595 | 0.640 | 14 | 104780214 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
| rs112445441 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 2 | |||
| rs7412 | 0.641 | 0.640 | 19 | 44908822 | missense variant | C/T | snv | 6.2E-02 | 7.9E-02 | 1 | |
| rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 1 | ||
| rs116150891 | 1.000 | 0.040 | 9 | 21970929 | missense variant | G/A;C | snv | 5.6E-04 | 2.6E-03 | 1 | |
| rs6413464 | 1.000 | 0.040 | 9 | 21970980 | missense variant | C/A;G | snv | 1.3E-03; 4.1E-06 | 1 | ||
| rs121913082 | 1.000 | 0.040 | 10 | 89014205 | missense variant | A/G | snv | 1 | |||
| rs121913083 | 1.000 | 0.040 | 10 | 89008907 | missense variant | A/G | snv | 1 | |||
| rs121913084 | 1.000 | 0.040 | 10 | 89010779 | missense variant | T/C | snv | 1 | |||
| rs351855 | 0.597 | 0.560 | 5 | 177093242 | missense variant | G/A | snv | 0.33 | 0.26 | 1 | |
| rs861539 | 0.519 | 0.680 | 14 | 103699416 | missense variant | G/A | snv | 0.29 | 0.30 | 1 | |
| rs201125580 | 1.000 | 0.040 | 9 | 95467191 | missense variant | C/A;T | snv | 4.0E-06; 3.8E-04 | 1 | ||
| rs779417284 | 1.000 | 0.040 | 9 | 95449149 | missense variant | C/T | snv | 2.4E-05 | 1 | ||
| rs59912467 | 0.790 | 0.120 | 19 | 1223126 | missense variant | C/G;T | snv | 5.2E-03; 4.1E-06 | 1 | ||
| rs762846821 | 0.614 | 0.320 | 17 | 7675151 | missense variant | C/A;T | snv | 8.0E-06 | 1 |