| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs80338796 | 0.667 | 0.480 | 3 | 12604200 | missense variant | G/A;C | snv | 4.0E-06 | 37 | ||
| rs121434594 | 0.827 | 0.160 | 3 | 12604189 | missense variant | G/A;C;T | snv | 5 | |||
| rs397516830 | 0.827 | 0.160 | 3 | 12604182 | missense variant | A/C;G;T | snv | 5 | |||
| rs587777587 | 1.000 | 3 | 12584539 | missense variant | G/A;C | snv | 1.2E-05; 4.0E-06 | 1.4E-05 | 2 | ||
| rs1057403865 | 1.000 | 3 | 12599805 | missense variant | G/C | snv | 7.0E-06 | 1 | |||
| rs1553609795 | 1.000 | 3 | 12584584 | missense variant | T/C | snv | 1 | ||||
| rs587777586 | 1.000 | 3 | 12584653 | missense variant | A/G | snv | 1 | ||||
| rs587777588 | 1.000 | 3 | 12604261 | missense variant | C/T | snv | 1.6E-05 | 1.4E-05 | 1 | ||
| rs778155315 | 1.000 | 3 | 12600214 | missense variant | T/C | snv | 8.0E-06 | 1 |