| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs61753793 | 0.851 | 0.120 | 2 | 47799002 | missense variant | T/C | snv | 3.6E-05 | 5.6E-05 | 3 | |
| rs74315450 | 0.851 | 0.120 | 21 | 34859485 | missense variant | C/T | snv | 1 | |||
| rs104894421 | 0.882 | 0.200 | 13 | 108210436 | missense variant | C/A;T | snv | 1.2E-05 | 2 | ||
| rs121909629 | 0.882 | 0.200 | 8 | 38415905 | missense variant | C/T | snv | 1 | |||
| rs397507476 | 0.882 | 0.200 | 7 | 140778011 | missense variant | T/A;G | snv | 1 | |||
| rs6413463 | 1.000 | 0.040 | 9 | 21970990 | missense variant | A/G;T | snv | 2.9E-05; 3.0E-04 | 1 |