| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121909627 | 0.776 | 0.200 | 8 | 38424690 | missense variant | G/C | snv | 4.0E-06 | 2 | ||
| rs779707422 | 0.763 | 0.280 | 8 | 38417331 | missense variant | G/A;T | snv | 4.0E-06 | 1 | ||
| rs869320694 | 0.742 | 0.520 | 8 | 38414790 | missense variant | T/C | snv | 1 | |||
| rs121909633 | 1.000 | 0.080 | 8 | 38424546 | missense variant | A/G | snv | 2.9E-04 | 4.1E-04 | 1 | |
| rs121909631 | 0.827 | 0.280 | 8 | 38419696 | missense variant | T/C | snv | 1 | |||
| rs121909632 | 1.000 | 0.080 | 8 | 38421889 | missense variant | T/A;C | snv | 4.0E-06 | 1 | ||
| rs121909634 | 1.000 | 0.080 | 8 | 38419676 | missense variant | A/G | snv | 1 | |||
| rs886037634 | 0.925 | 0.160 | 8 | 38421836 | missense variant | C/T | snv | 1 | |||
| rs1554570706 | 0.925 | 0.200 | 8 | 38429808 | missense variant | G/A | snv | 1 | |||
| rs121909628 | 0.925 | 0.160 | 8 | 38414892 | stop gained | G/A;C | snv | 1 | |||
| rs121909635 | 0.827 | 0.240 | 8 | 38426158 | missense variant | C/T | snv | 1 | |||
| rs121909641 | 0.763 | 0.520 | 8 | 38419720 | missense variant | G/A | snv | 1 | |||
| rs781328162 | 0.925 | 0.160 | 8 | 38413714 | missense variant | C/T | snv | 2.0E-05 | 3.5E-05 | 1 | |
| rs121909642 | 0.925 | 0.160 | 8 | 38414174 | missense variant | G/A | snv | 1 | |||
| rs397515446 | 0.925 | 0.160 | 8 | 38414599 | missense variant | C/T | snv | 1 | |||
| rs121909630 | 0.925 | 0.160 | 8 | 38428043 | missense variant | C/A | snv | 1 | |||
| rs121909638 | 0.882 | 0.280 | 8 | 38421853 | missense variant | A/G | snv | 1 | |||
| rs780765366 | 1.000 | 0.160 | 8 | 38429690 | missense variant | T/C | snv | 6.1E-05 | 4.9E-05 | 1 | |
| rs121909640 | 0.925 | 0.160 | 8 | 38429898 | missense variant | C/T | snv | 1 | |||
| rs749758370 | 1.000 | 0.160 | 8 | 38417411 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs55642501 | 1.000 | 0.160 | 8 | 38429736 | missense variant | C/T | snv | 4.2E-04 | 1.7E-04 | 1 | |
| rs727505373 | 0.925 | 0.160 | 8 | 38429744 | missense variant | T/C | snv | 1 | |||
| rs765615419 | 1.000 | 0.160 | 8 | 38428408 | missense variant | T/C;G | snv | 1.4E-04 | 1 | ||
| rs121909637 | 0.882 | 0.240 | 8 | 38418249 | missense variant | C/A;T | snv | 1.2E-05; 2.0E-05 | 1 | ||
| rs121909629 | 0.882 | 0.200 | 8 | 38415905 | missense variant | C/T | snv | 1 |