Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs111033205 | 0.882 | 0.240 | 7 | 107661726 | stop gained | G/C;T | snv | 9.3E-05; 6.2E-06 | 4 | ||
| rs1057517303 | 0.925 | 0.160 | 7 | 107710192 | stop gained | T/A;C | snv | 3 | |||
| rs121908361 | 0.882 | 0.160 | 7 | 107689156 | stop gained | A/G;T | snv | 3 | |||
| rs747076316 | 0.925 | 0.160 | 7 | 107694622 | stop gained | C/A;G;T | snv | 2.0E-05 | 2.1E-05 | 3 | |
| rs752807925 | 0.925 | 0.160 | 7 | 107704382 | stop gained | C/T | snv | 1.3E-05 | 3 | ||
| rs786204581 | 0.925 | 0.160 | 7 | 107663366 | stop gained | C/T | snv | 3 | |||
| rs370588279 | 0.925 | 0.160 | 7 | 107663400 | stop gained | C/A;T | snv | 4.0E-06; 2.0E-05 | 2 | ||
| rs1057516658 | 1.000 | 0.160 | 7 | 107663380 | stop gained | G/A | snv | 1 | |||
| rs1057516678 | 1.000 | 0.160 | 7 | 107674963 | stop gained | C/T | snv | 4.0E-06 | 1 | ||
| rs111033200 | 1.000 | 0.160 | 7 | 107663301 | stop gained | C/A;G | snv | 1.2E-05 | 1 | ||
| rs142656144 | 1.000 | 0.160 | 7 | 107710082 | stop gained | C/A;T | snv | 8.0E-06; 3.2E-05 | 1 | ||
| rs1554359693 | 1.000 | 0.160 | 7 | 107694694 | stop gained | G/A | snv | 1 | |||
| rs1554361584 | 1.000 | 0.160 | 7 | 107704340 | stop gained | G/T | snv | 1 | |||
| rs201636911 | 1.000 | 0.160 | 7 | 107661783 | stop gained | G/A;T | snv | 3.5E-05 | 1 | ||
| rs368119540 | 1.000 | 0.160 | 7 | 107701943 | stop gained | G/A;C;T | snv | 1.2E-05; 4.0E-06 | 1 | ||
| rs397516416 | 1.000 | 0.160 | 7 | 107694475 | stop gained | C/T | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs397516430 | 1.000 | 0.160 | 7 | 107661709 | stop gained | C/A;T | snv | 1 | |||
| rs727503431 | 1.000 | 0.160 | 7 | 107710179 | stop gained | C/T | snv | 4.0E-06 | 1 | ||
| rs778901860 | 1.000 | 0.160 | 7 | 107701161 | stop gained | A/T | snv | 8.0E-06 | 1 | ||
| rs786204502 | 1.000 | 0.160 | 7 | 107701942 | stop gained | G/A | snv | 1 | |||
| rs111033307 | 0.851 | 0.240 | 7 | 107694473 | missense variant | T/G | snv | 1.0E-04 | 7.7E-05 | 6 | |
| rs80338848 | 0.851 | 0.240 | 7 | 107675051 | missense variant | T/C | snv | 2.7E-04 | 3.4E-04 | 6 | |
| rs111033243 | 0.827 | 0.400 | 7 | 107689112 | missense variant | T/C | snv | 6.1E-04 | 8.1E-04 | 5 | |
| rs121908362 | 0.882 | 0.280 | 7 | 107710132 | missense variant | A/G | snv | 1.2E-04 | 3.5E-05 | 5 | |
| rs111033212 | 0.851 | 0.240 | 7 | 107689054 | missense variant | T/A;C | snv | 4.0E-06; 8.6E-04 | 4 |