| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs111033178 | 0.851 | 0.200 | 11 | 77190108 | missense variant | G/A | snv | 7.5E-05 | 5.6E-05 | 6 | |
| rs111033437 | 0.882 | 0.120 | 11 | 77179925 | missense variant | G/A;T | snv | 6 | |||
| rs111033201 | 0.851 | 0.200 | 11 | 77174825 | stop gained | C/A;G;T | snv | 4.0E-06; 4.0E-06; 1.6E-05 | 4 | ||
| rs750647872 | 0.851 | 0.200 | 11 | 77192132 | stop gained | C/T | snv | 3.2E-05 | 4 | ||
| rs1057517857 | 0.882 | 0.200 | 11 | 77190113 | stop gained | C/T | snv | 3 | |||
| rs111033180 | 0.882 | 0.200 | 11 | 77172850 | stop gained | C/A;T | snv | 1.4E-05 | 3 | ||
| rs111033214 | 0.882 | 0.200 | 11 | 77189348 | missense variant | G/A | snv | 2.0E-05 | 4.2E-05 | 3 | |
| rs111033283 | 0.882 | 0.200 | 11 | 77156909 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 3 | |
| rs368657015 | 0.882 | 0.200 | 11 | 77205554 | missense variant | T/C | snv | 2.4E-05 | 7.0E-06 | 3 | |
| rs755934966 | 0.882 | 0.200 | 11 | 77208780 | missense variant | G/A | snv | 1.1E-05 | 6.3E-05 | 3 | |
| rs766641715 | 0.882 | 0.200 | 11 | 77192243 | stop gained | C/T | snv | 1.2E-05 | 7.0E-06 | 3 | |
| rs878853236 | 0.882 | 0.200 | 11 | 77174789 | missense variant | C/T | snv | 4.2E-06 | 3 | ||
| rs121965084 | 1.000 | 0.120 | 11 | 77162149 | missense variant | A/G;T | snv | 1.3E-05 | 2 | ||
| rs201539845 | 1.000 | 0.120 | 11 | 77156921 | missense variant | G/A | snv | 4.4E-05 | 5.6E-05 | 1 | |
| rs782808261 | 1.000 | 0.120 | 11 | 77156060 | missense variant | C/T | snv | 8.0E-06 | 1 | ||
| rs797044512 | 1.000 | 0.120 | 11 | 77156958 | missense variant | C/T | snv | 1 |