| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs747842199 | 1.000 | 0.160 | 8 | 38429694 | missense variant | C/T | snv | 2.8E-05 | 1.4E-05 | 1 | |
| rs398122945 | 1.000 | 0.280 | 8 | 38414164 | missense variant | C/T | snv | 1 | |||
| rs1554570706 | 0.925 | 0.200 | 8 | 38429808 | missense variant | G/A | snv | 1 | |||
| rs121909641 | 0.763 | 0.520 | 8 | 38419720 | missense variant | G/A | snv | 1 | |||
| rs121909642 | 0.925 | 0.160 | 8 | 38414174 | missense variant | G/A | snv | 1 | |||
| rs121913473 | 1.000 | 0.080 | 8 | 38428420 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs121909628 | 0.925 | 0.160 | 8 | 38414892 | stop gained | G/A;C | snv | 1 | |||
| rs779707422 | 0.763 | 0.280 | 8 | 38417331 | missense variant | G/A;T | snv | 4.0E-06 | 1 | ||
| rs397515444 | 0.925 | 0.160 | 8 | 38417975 | missense variant | G/A;T | snv | 4.0E-06 | 1 | ||
| rs121909627 | 0.776 | 0.200 | 8 | 38424690 | missense variant | G/C | snv | 4.0E-06 | 2 | ||
| rs121909632 | 1.000 | 0.080 | 8 | 38421889 | missense variant | T/A;C | snv | 4.0E-06 | 1 | ||
| rs869320694 | 0.742 | 0.520 | 8 | 38414790 | missense variant | T/C | snv | 1 | |||
| rs121909631 | 0.827 | 0.280 | 8 | 38419696 | missense variant | T/C | snv | 1 | |||
| rs780765366 | 1.000 | 0.160 | 8 | 38429690 | missense variant | T/C | snv | 6.1E-05 | 4.9E-05 | 1 | |
| rs727505373 | 0.925 | 0.160 | 8 | 38429744 | missense variant | T/C | snv | 1 | |||
| rs727505369 | 0.925 | 0.160 | 8 | 38424624 | missense variant | T/C | snv | 1 | |||
| rs1085307879 | 1.000 | 0.160 | 8 | 38414183 | missense variant | T/C | snv | 1 | |||
| rs397515445 | 0.807 | 0.280 | 8 | 38414263 | missense variant | T/C | snv | 1 | |||
| rs765615419 | 1.000 | 0.160 | 8 | 38428408 | missense variant | T/C;G | snv | 1.4E-04 | 1 |