| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs36116683 | 15 | 70518645 | regulatory region variant | A/G | snv | 0.27 | 1 | ||||
| rs13047590 | 21 | 45143905 | intron variant | C/T | snv | 0.19 | 1 | ||||
| rs1377817 | 19 | 50300809 | intron variant | T/G | snv | 0.15 | 1 | ||||
| rs6759709 | 2 | 2043625 | intron variant | A/G | snv | 0.28 | 1 | ||||
| rs150691387 | 7 | 96538498 | intron variant | A/G | snv | 7.8E-03 | 1 | ||||
| rs61878760 | 11 | 12785642 | intron variant | G/A;C;T | snv | 1 | |||||
| rs138013532 | 4 | 182631880 | intron variant | C/T | snv | 5.9E-03 | 1 |