Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
| rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
| rs121913355 | 0.641 | 0.520 | 7 | 140781602 | missense variant | C/A;G;T | snv | 4.0E-06 | 42 | ||
| rs121913348 | 0.763 | 0.480 | 7 | 140781617 | missense variant | C/A;G;T | snv | 20 | |||
| rs121913366 | 0.763 | 0.400 | 7 | 140753345 | missense variant | A/C;T | snv | 12 | |||
| rs121913369 | 0.790 | 0.280 | 7 | 140753346 | missense variant | G/A;C | snv | 4.0E-06 | 12 | ||
| rs121913351 | 0.776 | 0.240 | 7 | 140781611 | missense variant | C/A;G;T | snv | 4.0E-06 | 9 | ||
| rs180177042 | 0.807 | 0.280 | 7 | 140749365 | missense variant | A/C;T | snv | 8 | |||
| rs1225976306 | 0.807 | 0.160 | 7 | 140924673 | missense variant | C/T | snv | 9.3E-06 | 8 | ||
| rs387906660 | 0.790 | 0.280 | 7 | 140801550 | missense variant | G/A;C;T | snv | 7 | |||
| rs387906661 | 0.807 | 0.280 | 7 | 140801551 | missense variant | T/G | snv | 6 | |||
| rs397507466 | 0.807 | 0.280 | 7 | 140801537 | missense variant | T/A;C;G | snv | 4.0E-06 | 6 | ||
| rs397516895 | 0.827 | 0.280 | 7 | 140753392 | missense variant | A/T | snv | 5 | |||
| rs1057519720 | 0.851 | 0.080 | 7 | 140781602 | missense variant | CC/AA;GA | mnv | 4 | |||
| rs868021367 | 0.882 | 0.080 | 7 | 140753319 | missense variant | C/G | snv | 3 | |||
| rs1057519719 | 1.000 | 0.080 | 7 | 140781593 | missense variant | T/C | snv | 2 |